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Showing all entries assigned as Structural Haemoglobinopathy (Show All):
IthaID | Common Name | Hb Name | HGVS Name | Genes | Functionality | Phenotype | Locus | Position |
---|---|---|---|---|---|---|---|---|
3027 | Init CD ATG>ATT [Met>Ile] | Hb Valdecilla | HBA2:c.3G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33778 |
431 | CD 1 GTG>ATG [Val>Met] | Hb A2-Fontanabuona | HBA2:c.4G>A | α2 | Causative | α-chain variant | NG_000006.1 | 33779 |
2306 | CD 1 GTG>CTG (Val>Leu) | Hb St. Josef | HBA2:c.4G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33779 |
432 | CD 1 GTG>GGG [Val>Gly] | Hb Antananarivo | HBA1:c.5T>G | HBA2:c.5T>G | α1, α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33780, 37584 |
433 | CD 1 GTG>GAG [Val>Glu] | Hb Thionville | HBA1:c.5T>A | HBA2:c.5T>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33780, 37584 |
434 | CD 1 GTG>GCG [Val>Ala] | Hb Lyon-Bron | HBA2:c.5T>C | α2 | Causative | α-chain variant | NG_000006.1 | 33780 |
2361 | CD 2 CTG>CCG [Leu>Pro] | Hb Kaiser West End | HBA2:c.8T>C | α2 | Causative | α-chain variant | NG_000006.1 | 33783 |
436 | CD 3 TCT>CCT [Ser>Pro] | Hb Central Middlesex | HBA1:c.10T>C | HBA2:c.10T>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33785, 37589 |
2371 | CD 3 TCT>TGT [Ser>Cys] | Hb Teterboro | HBA2:c.11C>G | α2 | Causative | α-chain variant | NG_000006.1 | 33786 |
2489 | CD 3 TCT>TAT [Ser>Tyr] | Hb Tallahassee | HBA2:c.11C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33786 |
438 | CD 4 CCT>CGT [Pro>Arg] | Hb Gorée | HBA2:c.14C>G | α2 | Causative | α-chain variant | NG_000006.1 | 33789 |
439 | CD 4 CCT>CAT [Pro>His] | Hb Bellevue | HBA2:c.14C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33789 |
440 | CD 5 GCC>CCC [Ala>Pro] | Hb Karachi | HBA1:c.16G>C | HBA2:c.16G>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33791, 37595 |
3983 | CD 5 GCC>ACC [Ala>Thr] | Hb Hengqin II | HBA2:c.16G>A | α2 | Causative | α-chain variant | NG_000006.1 | 33791 |
443 | CD 6 GAC>AAC [Asp>Asn] | Hb Dunn | HBA1:c.19G>A | HBA2:c.19G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33794, 37598 |
445 | CD 6 GAC>CAC [Asp>His] | Hb Galliera II | HBA2:c.19G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33794 |
446 | CD 6 -GAC [-Asp] | Hb Boyle Heights | HBA1:c.19_21delGAC | HBA2:c.19_21delGAC | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33794, 37598 |
3038 | CD 6 GAC>TAC [Asp>Tyr] | Hb Woodville | HBA2:c.19G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33794 |
447 | CD 6 GAC>GGC [Asp>Gly] | Hb Swan River | HBA2:c.20A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33795 |
448 | CD 6 GAC>GTC [Asp>Val] | Hb Ferndown | HBA1:c.20A>T | HBA2:c.20A>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33795, 37599 |
449 | CD 6 GAC>GCC [Asp>Ala] | Hb Sawara | HBA1:c.20A>C | HBA2:c.20A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33795, 37599 |
2383 | CD 7 AAG>CAG [Lys>Gln] | Hb J-Brainerd | HBA2:c.22A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33797 |
3762 | CD 7 AAG>GAG [Lys>Glu] | Hb Kurosaki | NM_000517.6(HBA2):c.22A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33797 |
451 | CD 7 AAG>AGG [Lys>Arg] | Hb Guanajuato | HBA2:c.23A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33798 |
2384 | CD 7 AAG>ACG [Lys>Thr] | Hb Nayarit | HBA2:c.23A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33798 |
452 | CD 7 AAG>AAC [Lys>Asn] | Hb Tatras | HBA1:c.24G>C | HBA2:c.24G>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33799, 37603 |
454 | CD 9 AAC>AGC [Asn>Ser] | Hb Zurich-Hottingen | HBA2:c.29A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33804 |
455 | CD 9 AAC>ACC [Asn>Thr] | Hb Broomfield | HBA1:c.29A>C | HBA2:c.29A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33804, 37608 |
457 | CD 9 AAC>AAG [Asn>Lys] | Hb Park Ridge | HBA2:c.30C>G | α2 | Causative | α-chain variant | NG_000006.1 | 33805 |
3402 | CD 9 AAC>AAA [Asn>Lys] | Hb Zhaoqing | HBA2:c.30C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33805 |
458 | CD 11 AAG>CAG [Lys>Gln] | Hb J-Wenchang-Wuming | HBA2:c.34A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33809 |
459 | CD 11 AAG>CAG [Lys>Glu] | Hb Anantharaj | HBA2:p.Lys12Glu | HBA1:p.Lys12Glu | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33809, 37613 |
3791 | CD 11 AAG>GAG [Lys>Glu] | Hb Arbresle | HBA2:c.34A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33809 |
3713 | CD 11 AAG>ACG [Lys>Thr] | N/A | HBA2:c.35A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33810 |
460 | CD 11 AAG>AAC or AAT [Lys>Asn] | Hb Albany-Suma | HBA1:c.36G>C | HBA1:c.36G>T | HBA2:c.36G>C | HBA2:c.36G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33811, 37615 |
2499 | CD 12 GCC>GAC [Ala>Asp] (Hb J-Aljezur) | Hb J-Paris-I | HBA1:c.38C>A | α1 | Causative | α-chain variant | NG_000006.1 | 33813 |
462 | CD 13 GCC>CCC [Ala>Pro] | Hb Ravenscourt Park | HBA1:c.40G>C | HBA2:c.40G>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33815, 37619 |
2977 | CD 13 GCC>GAC [Ala>Asp] | Hb Little Waltham | HBA2:c.41C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33816 |
3984 | CD 13 GCC>GTC [Ala>Val] | Hb Huidong | HBA2:c.41C>T | α2 | Causative | α-chain variant | NG_000006.1 | 33816 |
2348 | CD 14 TGG>TTG [Trp>Leu] | N/A | HBA2:c.44G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33819 |
3941 | CD 14 TGG>TCG [Trp>Ser] | Hb Jax | HBA2:c.44G>C | α2 | Causative | β-chain variant | NG_000006.1 | 33819 |
464 | CD 14 TGG>TGC [Trp>Cys] | Hb Bladensburg | HBA2:c.45G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33820 |
3761 | CD 15 GGT>CGT [Gly>Arg] | Hb Ottawa | HBA2:c.46G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33821 |
3916 | CD 15 GGT>TGT [Gly>Cys] | Hb Orbassano | HBA2:c.46G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33821 |
3487 | CD 15 GGT>GTT [Gly>Val] | Hb Liaoning | HBA2:c.47G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33822 |
467 | CD 16 AAG>GAG [Lys>Glu] (Hb I-Burlington, Hb I-Philadelphia, Hb I-Skamania, Hb I-Texas) | HbI | HBA2:c.49A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33824 |
469 | CD 16 AAG>ACG [Lys>Thr] | Hb Boa Esperanca | HBA2:c.50A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33825 |
470 | CD 16 AAG>AAT [Lys>Asn] | Hb Beijing | HBA2:c.51G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33826 |
3064 | CD 17 GTC>TTC [Val>Phe] | Hb Dapu | HBA2:c.52G>T | α2 | Causative | α-chain variant | NG_000006.1 | 33827 |
2978 | CD 17 GTC>GAC [Val>Asp] | Hb Oxford | HBA2:c.53T>A | α2 | Causative | α-chain variant | NG_000006.1 | 33828 |
3037 | CD 18 GGC>CGC [Gly>Arg] | Hb Handsworth | HBA2:c.55G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33830 |
472 | CD 18 GGC>GAC [Gly>Asp] | Hb Al-Ain Abu Dhabi | HBA1:c.56G>A | HBA2:c.56G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33831, 37635 |
473 | CD 19 GCG>GAG [Ala>Glu] | Hb J-Tashikuergan | HBA2:c.59C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33834 |
474 | CD 19 GCG>GAY [Ala>Asp] | Hb J-Kurosh | HBA2:c.59_60delinsAY^HBA1:c.59_60delinsAY | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33834, 37638 |
3715 | CD 19 GCG>GTG [Ala>Val] | N/A | HBA2:c.59C>T | α2 | Causative | α-chain variant | NG_000006.1 | 33834 |
475 | CD 20 CAC>TAC [His>Tyr] | Hb Necker Enfants-Malades | HBA1:c.61C>T | HBA2:c.61C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33836, 37640 |
476 | CD 20 CAC>GAC [His>Asp] | Hb Nikaia | HBA2:c.61C>G | α2 | Causative | α-chain variant | NG_000006.1 | 33836 |
478 | CD 20 CAC>CGC [His>Arg] | Hb Hobart | HBA1:c.62A>G | HBA2:c.62A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33837, 37641 |
3989 | CD 20 CAC>CTC [His>Leu] | Hb Hebei | HBA2: c.62A>T | α2 | Causative | α-chain variant | NG_000006.1 | 33837 |
479 | CD 20 CAC>CAA [His>Gln] | Hb Le Lamentin | HBA2:c.63C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33838 |
481 | CD 21 GCT>CCT [Ala>Pro] | Hb Fontainebleau | HBA2:c.64G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33839 |
2351 | CD 21 GCT>GTT [Ala>Val] | Hb Venetia | HBA2:c.65C>T | α2 | Causative | α-chain variant | NG_000006.1 | 33840 |
483 | CD 22 GGC>GAC [Gly>Asp] | Hb J-Medellin | HBA1:c.68G>A | HBA2:c.68G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33843, 37647 |
2438 | CD 22-26 (-9 bp) | Hb Zhanjiang | HBA2:c.69_77delCGAGTATGG | α2 | Causative | α-chain variant | NG_000006.1 | 33844 |
484 | CD 23 GAG>CAG [Glu>Gln] | Hb Memphis | HBA2:c.70G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33845 |
485 | CD 23 GAG>AAG [Glu>Lys] (Hb E-Keelung) | Hb Chad | HBA2:c.70G>A | α2 | Causative | α-chain variant | NG_000006.1 | 33845 |
486 | CD 23 GAG>GGG [Glu>Gly] | Hb Reims | HBA1:c.71A>G | HBA2:c.71A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33846, 37650 |
487 | CD 23 GAG>GTG [Glu>Val] | Hb G-Audhali | HBA1:c.71A>T | HBA2:c.71A>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33846, 37650 |
2368 | CD 23 GAG>GCG [Glu>Ala] | Hb Dayton | HBA2:c.71A>C | α2 | Causative | α-chain variant | NG_000006.1 | 33846 |
488 | CD 23 GAG>GAT [Glu>Asp] | Hb Lisbon | HBA1:c.72G>T | HBA2:c.72G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33847, 37651 |
489 | CD 24 TAT>CAT [Tyr>His] | Hb Luxembourg | HBA1:c.73T>C | HBA2:c.73T>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33848, 37652 |
490 | CD 24 TAT>GAT [Tyr>Asp] | Hb Creve Coeur | HBA2:c.73T>G | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 33848 |
3985 | CD 25 GGT>AGT [Gly>Ser] | Hb Jinwan | HBA2:c.76G>A | α2 | Causative | α-chain variant | NG_000006.1 | 33851 |
493 | CD 26 GCG>GTG [Ala>Val] | Hb Campinas | HBA2:c.80C>T | α2 | Causative | α-chain variant | NG_000006.1 | 33855 |
494 | CD GCG>GAG [Ala>Glu] | Hb Shenyang | HBA2:c.80C>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 33855 |
495 | CD 27 GAG>AAG [Glu>Lys] | Hb Shuangfeng | HBA2:c.82G>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 33857 |
496 | CD 27 GAG>GGG [Glu>Gly] | Hb Fort Worth | HBA2:c.83A>G | α2 | Causative | α-chain variant | NG_000006.1 | 33858 |
497 | CD 27 GAG>GTG [Glu>Val] | Hb Spanish Town | HBA2:c.83A>T | α2 | Causative | α-chain variant | NG_000006.1 | 33858 |
498 | CD 27 GAG>GCG [Glu>Ala] | Hb Hackney | HBA1:c.83A>C | HBA2:c.83A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 33858, 37662 |
499 | CD 27 GAG>GAC [Glu>Asp] | Hb Hekinan | HBA2:c.84G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33859 |
503 | CD 30 GAG>AAG [Glu>Lys] | Hb O-Padova | HBA2:c.91G>A | α2 | Causative | α-chain variant | NG_000006.1 | 33866 |
3766 | CD 30 GAG>CAG [Glu>Gln] | Hb G-Honolulu | HBA2:c.91G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33866 |
506 | CD 31 AGG>AGC [Arg>Ser] | Hb Prato | HBA2:c.96G>C | α2 | Causative | α-chain variant | NG_000006.1 | 33988 |
3363 | CD 33 TTC>CTC [Phe>Leu] | Hb Worthing | HBA2:c.100T>C | α2 | Causative | α-chain variant | NG_000006.1 | 33992 |
3362 | CD 34 CTG>CCG [Leu>Pro] | Hb Bass Hill | HBA2:c.104T>C | α2 | Causative | α-chain variant | NG_000006.1 | 33996 |
511 | CD 35 TCC>TAC [Ser>Tyr] | Hb Shinagawa | HBA2:c.107C>A | α2 | Causative | α-chain variant | NG_000006.1 | 33999 |
2999 | CD 35 TCC>TTC [Ser>Phe] | Hb Colorado | HBA2:c.107C>T | α2 | Causative | α-chain variant | NG_000006.1 | 33999 |
512 | CD 36 TTC>CTC [Phe>Leu] | Hb Geisinger | HBA2:c.109T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34001 |
2373 | CD 37 CCC>TCC [Pro>Ser] | Hb Boskoop | HBA2:c.112C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34004 |
514 | CD 37 CCC>CTC [Pro>Leu] | Hb Manawatu | HBA2:c.113C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34005 |
515 | CD 37 CCC>CGC [Pro>Arg] | Hb Boumerdes | HBA2:c.113C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34005 |
516 | CD 37 +GAA [+Glu] | Hb Catonsville | HBA1:c.114_115insGAA | HBA2:c.114_115insGAA | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34006, 37810 |
2319 | CD 38 ACC>GCC [Thr>Ala] | Hb Beaconsfield | HBA1:c.115A>G | HBA2:c.115A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34007, 37811 |
3488 | CD 38 ACC>AAC [Thr>Asn] | Hb Pescara | HBA2:c.116C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34008 |
519 | CD 40 AAG>GAG [Lys>Glu] | Hb Kariya | HBA1:c.121A>G | HBA2:c.121A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34013, 37817 |
520 | CD 40 AAG>CAG [Lys>Gln] | Hb Linwood | HBA2:c.121A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34013 |
521 | CD 40 AAG>ATG [Lys>Met] | Hb Kanagawa | HBA2:c.122A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34014 |
524 | CD 40 AAG>AAC [Lys>Asn] | Hb Villiers le Bel | HBA2:c.123G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34015 |
525 | CD 41 ACC>TCC or AGC [Thr>Ser] | Hb Miyano | HBA1:c.124A>T | HBA1:c.125C>G | HBA2:c.124A>T | HBA2:c.125C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34016, 37820 |
3986 | CD 41 ACC>AAC [Thr>Asn] | Hb Zhuhai | HBA2:c.125C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34017 |
3489 | CD 42 TAC>GAC [Tyr>Asp] | Hb Huaxi | HBA2:c.127T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34019 |
3801 | CD 42 TAC>TGC [Tyr>Cys] | Hb Hauteluce | HBA2:c.128A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34020 |
527 | CD 43 TTC>GTC [Phe>Val] | Hb Torino | HBA1:c.130T>G | HBA2:c.130T>G | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34022, 37826 |
528 | CD 43 TTC>ATC [Phe>Ile] | Hb Sens | HBA2:c.130T>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34022 |
529 | CD 43 TTC>TTG [Phe>Leu] | Hb Hirosaki | HBA2:c.132C>G | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34024 |
3382 | CD 44 CCG>TCG [Pro>Ser] | Hb Xuchang | HBA2:c.133C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34025 |
3763 | CD 44 CCG>GCG [Pro>Ala] | Hb Milne | HBA2:c.133C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34025 |
532 | CD 44 CCG>CGG [Pro>Arg] | Hb Kawachi | HBA1:c.134C>G | HBA2:c.134C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34026, 37830 |
533 | CD 44 CCG>CTG [Pro>Leu] | Hb Milledgeville | HBA2:c.134C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34026 |
534 | CD 45 CAC>TAC [His>Tyr] | Hb Matsudo | HBA1:c.136C>T | HBA2:c.136C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34028, 37832 |
535 | CD 45 CAC>GAC [His>Asp] | Hb Poitiers | HBA1:c.136C>G | HBA2:c.136C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34028, 37832 |
537 | CD 45 CAC>CCC [His>Pro] | Hb Oita | HBA2:c.137A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34029 |
538 | CD 45 CAC>CAG [His>Gln] | Hb Bari | HBA2:c.138C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34030 |
2541 | CD 45 CAC>CAG [His>Gln]; CD 57 GGC>CGC [Gly>Arg] | Hb Blythe Boulevard | HBA2:c.[138C>G;172G>C] | α2 | Causative | α-chain variant | NG_000006.1 | 34030, 34064 |
539 | CD 46 TTC>TTG or TTA or CTC [Phe>Leu] | Hb Rockaway | HBA1:c.139T>C | HBA1:c.141C>A | HBA1:c.141C>G | HBA2:c.139T>C | HBA2:c.141C>A | HBA2:c.141C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34031, 37835 |
540 | CD 46 TTC>GTC [Phe>Val] | Hb Hillingdon | HBA1:c.139T>G | HBA2:c.139T>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34031, 37835 |
2953 | CD 46 TTC>ATC [Phe>Ile] | Hb Brigante | HBA2:c.139T>A | α2 | Causative | α-chain variant | NG_000006.1 | 34031 |
2376 | CD 46 TTC>TCC [Phe>Ser] | Hb Lake Tapawingo | HBA2:c.140T>C | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34032 |
541 | CD 47 GAC>CAC [Asp>His] (Hb L-Ferrara, Hb Michigan-I, Hb Michigan-II, Hb Sealy, Hb Sinai) | Hb Hasharon | HBA2:c.142G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34034 |
543 | CD 47 GAC>TAC [Asp>Tyr] | Hb Kurdistan | HBA2:c.142G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34034 |
4107 | CD 47 GAC>AAC [Asp>Asn] | Hb Arya | HBA2:c.142G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34034 |
544 | CD 47 GAC>GGC [Asp>Gly] (Hb Kokura , Hb L-Gaslini , Hb Mugino , Hb Tagawa-II , Hb Umi , Hb Yukuhashi-II) | Hb Beilinson | HBA1:c.143A>G | HBA2:c.143A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34035, 37839 |
545 | CD 47 GAC>GCC [Asp>Ala] | Hb Cordele | HBA1:c.143A>C | HBA2:c.143A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34035, 37839 |
546 | CD 48 CTG>CGG [Leu>Arg] | Hb Montgomery | HBA2:c.146T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34038 |
2535 | CD 48-54 -18 bp | Hb Fenton | HBA2:c.146_163delTGAGCCACGGCTCTGCCC | α2 | Causative | α-chain variant | NG_000006.1 | 34038 |
2955 | CD 49-57 (-24bp): (-GCCACGGCTCTGCCCAGGTTAAGG) | Hb Goya | HBA2:c.149_172del | α2 | Causative | α-chain variant | NG_000006.1 | 34041 |
548 | CD 49 AGC>AGA or AGG [Ser>Arg] | Hb Savaria | HBA2:c.150C>A |HBA2:c.150C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34042 |
549 | CD 50 CAC>GAC [His>Asp] | Hb J-Sardegna | HBA2:c.151C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34043 |
2314 | CD 50 CAC>TAC [His>Tyr] | Hb South Yorkshire | HBA1:c.151C>T | HBA2:c.151C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34043, 37847 |
551 | CD 50 CAC>CGC [His>Arg] | Hb Aichi | HBA1:c.152A>G | HBA2:c.152A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34044, 37848 |
3923 | CD 50 CAC>CCC [His>Pro] | Hb Porter Brook | HBA2:c.152A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34044 |
552 | CD 50 CAC>CAG [His>Gln] | Hb Frankfurt | HBA2:c.153C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34045 |
2511 | -α3.7;CD 50 CAC>CAG [His>Gln] (-α3.7kb Frankfurt) | Hb Frankfurt | NG_000006.1:g.34247_38050del;34045C>G | α3.7 hybrid | Causative | α-chain variant | NG_000006.1 | 34045 |
554 | CD 51 GGC>CGC [Gly>Arg] | Hb Russ | HBA2:c.154G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34046 |
2458 | CD 51 GGC>AGC [Gly>Ser] | Hb Riccarton II | HBA2:c.154G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34046 |
3397 | CD 51 GGC>TGC [Gly>Cys] | Hb Hunan | HBA2:c.154G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34046 |
555 | CD 51 GGC>GAC [Gly>Asp] | Hb J-Abidjan | HBA1:c.155G>A | HBA2:c.155G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34047, 37851 |
2423 | CD 52 TCT>GCT [Ser>Ala] | Hb Cheshire | HBA1:c.157T>G | HBA2:c.157T>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34049, 37853 |
3039 | CD 52-59 (-24bp): (-TCTGCCCAGGTTAAGGGCCACGGC) | Hb J-Biskra | HBA2: c.157_180del | α2 | Causative | α-chain variant | NG_000006.1 | 34049 |
557 | CD 52 TCT>TTT [Ser>Phe] | Hb Essex | HBA2:c.158C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34050 |
558 | CD 53 GCC>GAC [Ala>Asp] | Hb J-Rovigo | HBA2:c.161C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34053 |
2472 | CD 54 CAG>CCG [Gln>Pro] | Hb Dhaka | HBA1:c.164A>C | HBA2:c.164A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34056, 37860 |
2397 | CD 54 CAG>CAC or CAT [Gln>His] | Hb Princes Risborough | HBA1:p.[Gln55His] | HBA2:p.[Gln55His] | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34057, 37861 |
563 | CD 55 GTT>GCT [Val>Ala] | Hb Gerland | HBA2:c.167T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34059 |
564 | CD 56 AAG>GAG [Lys>Glu] | Hb Shaare Zedek | HBA2:c.169A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34061 |
565 | CD 56 AAG>AGG [Lys>Arg] | Hb Port Huron | HBA1:c.170A>G | HBA2:c.170A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34062, 37866 |
569 | CD 57 GGC>GAC [Gly>Asp] (Hb Kagoshima, Hb Nishik-I, Hb Nishik-II, Hb Nishik-III) | Hb J-Norfolk | HBA2:c.173G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34065 |
570 | CD 58 CAC>TAC [His>Tyr] (Hb M-Gothenburg, Hb M-Kiskunhalas, Hb M-Norin, Hb M-Osaka) | Hb M-Boston | HBA2:c.175C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34067 |
4072 | CD 58 CAC>AAC [His>Asn] | Hb DG-Nancheng | HBA2:c.175C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34067 |
571 | CD 58 CAC>CAA [His>Gln] | Hb Boghé | HBA2:c.177C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34069 |
2474 | CD 58 CAC>CAG [His>Gln] | Hb Flurlingen | HBA2:c.177C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34069 |
2409 | CD 59 GGC>AGC [Gly>Ser] | Hb Parma | HBA2:c.178G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34070 |
575 | CD 59 GGC>GTC [Gly>Val] | Hb Tottori | HBA1:c.179G>T | HBA2:c.179G>T | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34071, 37875 |
577 | CD 60 AAG>GAG [Lys>Glu] | Hb Dagestan | HBA2:c.181A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34073 |
3987 | CD 60 AAG>AGG [Lys>Arg] | Hb Liuzhou-Liyong | HBA2:c.182A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34074 |
580 | CD 61 AAG>GAG [Lys>Glu] | Hb Miyagi | HBA1:c.184A>G | HBA2:c.184A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34076, 37880 |
581 | CD 61 AAG>ACG [Lys>Thr] | Hb J-Anatolia | HBA2:c.185A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34077 |
583 | CD 62 GTG>ATG [Val>Met] | Hb Evans | HBA2:c.187G>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34079 |
2362 | CD 63 GCC>GTC [Ala>Val] (Hb Aberystwyth) | Hb Nakhon Ratchsima | HBA2:c.191C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34083 |
586 | CD 64 GAC>TAC [Asp>Tyr] | Hb Persepolis | HBA1:c.193G>T | HBA2:c.193G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34085, 37889 |
588 | CD 64 GAC>AAC [Asp>Asn] (Hb Aida) | Hb G-Waimanalo | HBA2:c.193G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34085 |
589 | CD 64 GAC>GGC [Asp>Gly] | Hb Guangzhou-Hangzhou | HBA1:c.194A>G | HBA2:c.194A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34086, 37890 |
590 | CD 65 GCG>ACG [Ala>Thr] | Hb Part-Dieu | HBA2:c.196G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34088 |
591 | CD 65 GCG>GTG [Ala>Val] | Hb Bois Guillaume | HBA1:c.197C>T | HBA2:c.197C>T | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34089, 37893 |
3381 | CD 67 ACC>ATC [Thr>Ile] | Hb Sichuan | HBA2:c.203C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34095 |
593 | CD 68 AAC>GAC [Asn>Asp] | Hb Ube-2 | HBA2:c.205A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34097 |
595 | CD 68 AAC>CAC [Asn>His] | Hb St. Truiden | HBA2:c.205A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34097 |
2318 | CD 68 AAC>TAC [Asn>Tyr] | Hb Chelmsford | HBA1:c.205A>T | HBA2:c.205A>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34097, 37901 |
596 | CD 68 AAC>AAA [Asn>Lys] (Hb D-Baltimore, Hb D-St. Louis, Hb D-Washington, Hb G-Azakouli, Hb G-Bristol, Hb G-Knoxville, Hb Stanleyville-I) | Hb G-Philadelphia | HBA2:c.207C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34099 |
598 | CD 69 GCC>ACC [Ala>Thr] | Hb Decines-Charpieu | HBA2:c.208G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34100 |
2335 | CD 70 GTG>GGG [Val>Gly] | Hb Edinburgh | HBA2:c.212T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34104 |
2312 | CD 71 GCG>ACG [Ala>Thr] | Hb Hatfield | HBA1:c.214G>A | HBA2:c.214G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34106, 37910 |
600 | CD 71 GCG>GAG [Ala>Glu] | Hb J-Habana | HBA1:c.215C>A | HBA2:c.215C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34107, 37911 |
602 | CD 72 CAC>GAC [His>Asp] | Hb Norton | HBA2:c.217C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34109 |
603 | CD 72 CAC>TAC [His>Tyr] (Hb Tanashi) | Hb Fuchu-I | HBA1:c.217C>T | HBA2:c.217C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34109, 37913 |
604 | CD 72 CAC>CGC [His>Arg] | Hb Daneshgah-Tehran | HBA2:c.218A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34110 |
605 | CD 72 CAC>CAA [His>Gln] | Hb Gouda | HBA2:c.219C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34111 |
606 | CD 74 GAC>AAC [Asp>Asn] | Hb G-Pest | HBA2:c.223G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34115 |
2979 | CD 74 GAC>TAC [ Asp>Tyr] | Hb Uttoxeter | HBA2:c.223G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34115 |
610 | CD 74 GAC>GCC [Asp>Ala] | Hb Lille | HBA1:c.224A>C | HBA2:c.224A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34116, 37920 |
3749 | CD 74 GAC>GGC [Asp>Gly] (Hb Chapel Hill) | Hb Liangqing | HBA2:c224A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34116 |
612 | CD 75 GAC>AAC [Asp>Asn] | Hb Matsue-Oki | HBA2:c.226G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34118 |
613 | CD 75 GAC>CAC [Asp>His] | Hb Q-Iran | HBA2:c.226G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34118 |
614 | CD 75 GAC>TAC [Asp>Tyr] | Hb Winnipeg | HBA2:c.226G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34118 |
615 | CD 75 GAC>GTC [Asp>Val] | Hb Al-Hammadi Riyadh | HBA2:c.227A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34119 |
616 | CD 75 GAC>GGC [Asp>Gly] | Hb Mizushi | HBA2:c.227A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34119 |
617 | CD 76 ATG>AGG [Met>Arg] | Hb Walpole | HBA1:c.230T>G | HBA2:c.230T>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34122, 37926 |
618 | CD 76 ATG>ACG [Met>Thr] | Hb Aztec | HBA2:c.230T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34122 |
619 | CD 76 ATG>AAG [Met>Lys] | Hb Noko | HBA1:c.230T>A | HBA2:c.230T>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34122, 37926 |
620 | CD 76 ATG>ATA [Met>Ile] | Hb Hellux | HBA2:c.231G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34123 |
2486 | CD 77 CCC>TCC [Pro>Ser] | Hb Nile | HBA2:c.232C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34124 |
621 | CD 77 CCC>CAC [Pro>His] | Hb Toulon | HBA2:c.233C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34125 |
622 | CD 77 CCC>CTC [Pro>Leu] | Hb Asklipios | HBA2:c.233C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34125 |
623 | CD 77 CCC>CGC [Pro>Arg] | Hb GuiZhou | HBA1:c.233C>G | HBA2:c.233C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34125, 37929 |
624 | CD 78 AAC>GAC [Asn>Asp] | Hb J-Singa | HBA1:c.235A>G | HBA2:c.235A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34127, 37931 |
626 | CD 78 AAC>AAG or AAA [Asn>Lys] | Hb Stanleyville-II | HBA2:c.[237C>A ;237C>G] | α2 | Causative | α-chain variant | NG_000006.1 | 34129 |
627 | CD 79 GCG>ACG [Ala>Thr] | Hb Mantes-La-Jolie | HBA1:c.238G>A | HBA2:c.238G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34130, 37934 |
628 | CD 79 GCG>GGG [Ala>Gly] | Hb J-Singapore | HBA2:c.239C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34131 |
629 | CD 80 CTG>GTG [Leu>Val] | Hb Conakry | HBA2:c.241C>G | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34133 |
630 | CD 80 CTG>CGG [Leu>Arg] | Hb Ann Arbor | HBA2:c.242T>G | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34134 |
3800 | CD 80 CTG>CCG [Leu>Pro] | Hb Robbinsdale | HBA2:c.242T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34134 |
631 | CD 81 TCC>CCC [Ser>Pro] | Hb Passy | HBA2:c.244T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34136 |
2980 | CD 81 TCC>TAC [Ser>Tyr] | Hb Wolverhampton | HBA2:c.245C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34137 |
3884 | CD 81 TCC>TTC [Ser>Phe] | Hb Zhaotong | HBA2:c.245C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34137 |
634 | CD 82 GCC>GAC [Ala>Asp] | Hb Garden State | HBA1:c.248C>A | HBA2:c.248C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34140, 37944 |
635 | CD 83 CTG>CCG [Leu>Pro] | Hb Les Andelys | HBA2:c.251T>C | α2 | Causative | α-chain variant | NG_000006.1 | 34143 |
636 | CD 84 AGC>GGC [Ser>Gly] | Hb Wembley | HBA1:c.253A>G | HBA2:c.253A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34145, 37949 |
638 | CD 84 AGC>AAC [Ser>Asn] | Hb Meulan | HBA2:c.254G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34146 |
2970 | CD 84 AGC>ACC [Ser>Thr] | Hb Oelsnitz | HBA2:c.254G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34146 |
640 | CD 85 GAC>TAC [Asp>Tyr] | Hb Atago | HBA1:c.256G>T | HBA2:c.256G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34148, 37952 |
2446 | CD 85 GAC>CAC [Asp>His] | Hb Canuts II | HBA2:c.256G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34148 |
3952 | CD 85 GAC>AAC [Asp>Asn] | Hb G-Norfolk | HBA2:c.256G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34148 |
642 | CD 85 GAC>GTC [Asp>Val] | Hb Inkster | HBA2:c.257A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34149 |
2355 | CD 85 GAC>GGC [Asp>Gly] | Hb Benton | HBA2:c.257A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34149 |
2398 | CD 85 GAC>GAA or GAG [Asp>Glu] | Hb Aylesbury | HBA1:c.258C>A | HBA1:c.258C>G | HBA2:c.258C>A | HBA2:c.258C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34150, 37954 |
2372 | CD 86 CTG>GTG [Leu>Val] | Hb Ridgewood | HBA2:c.259C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34151 |
643 | CD 86 CTG>CGG [Leu>Arg] | Hb Moabit | HBA1:c.260T>G | HBA2:c.260T>G | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34152, 37956 |
644 | CD 87 +9 bp [+Ser-Asp-Leu] | Hb Neuilly-sur-Marne | HBA1:c.253_261dup | HBA2:c.253_261dup | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34154, 37949 |
645 | CD 87 CAC>TAC [His>Tyr] (Hb M-Kankakee, Hb M-Oldenburg, Hb M-Sendai) | Hb M-Iwate | HBA2:c.262C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34154 |
646 | CD 87 CAC>AAC [His>Asn] | Hb Auckland | HBA1:c.262C>A | HBA2:c.262C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34154, 37958 |
648 | CD 87 CAC>CGC [His>Arg] | Hb Iwata | HBA1:c.263A>G | HBA2:c.263A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34155, 37959 |
2308 | CD 87 CAC>CAG [His>Gln] | Hb Lansing | HBA2:c.264C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34156 |
2549 | CD 87 CAC>CAA [His>Glu] | Hb Lansing (A) | HBA2:c.264C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34156 |
650 | CD 88 GCG>TCG [Ala>Ser] | Hb Loire | HBA1:c.265G>T | HBA2:c.265G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34157, 37961 |
2367 | CD 88 GCG>ACG [Ala>Thr] | Hb Voorhees | HBA2:c.265G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34157 |
651 | CD 88 GCG>GAG [Ala>Glu] | Hb Wroclaw | HBA1:c.266C>A | HBA2:c.266C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34158, 37962 |
652 | CD 88 GCG>GTG [Ala>Val] | Hb Columbia Missouri | HBA1:c.266C>T | HBA2:c.266C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34158, 37962 |
653 | CD 88 GCG>GGG [Ala>Gly] | Hb Valparaiso | HBA1:c.266C>G | HBA2:c.266C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34158, 37962 |
654 | CD 89 CAC>TAC [His>Tyr] | Hb Villeurbanne | HBA2:c.268C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34160 |
655 | CD 89 CAC>CCC [His>Pro] | Hb Tokyo | HBA1:c.269A>C | HBA2:c.269A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34161, 37965 |
656 | CD 89 CAC>CGC [His>Arg] | Hb Tamano | HBA1:c.269A>G | HBA2:c.269A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34161, 37965 |
657 | CD 89 CAC>CTC [His>Leu] | Hb Luton | HBA2:c.269A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34161 |
2390 | CD 89 CAC>CAG [His>Gln] | Hb Enfield | HBA2:c.270C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34162 |
659 | CD 90 AAG>GAG [Lys>Glu] | Hb Sudbury | HBA1:c.271A>G | HBA2:c.271A>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34163, 37967 |
2388 | CD 90 AAG>CAG [Lys>Gln] | Hb Bergerac | HBA2:c.271A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34163 |
660 | CD 90 AAG>ATG [Lys>Met] (Hb Munakata) | Hb Handa | HBA1:c.272A>T | HBA2:c.272A>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34164, 37968 |
661 | CD 90 AAG>AGG [Lys>Arg] | Hb Clinico-Madrid | HBA2:c.272A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34164 |
664 | CD 90 AAG>AAT (Hb Tagawa-I) | Hb J-Broussais | HBA2:c.273G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34165 |
2311 | CD 91 CTT>TTT [Leu>Phe] | Hb Treviso | HBA2: c.274C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34166 |
2470 | CD 91 CTT>ATT [Leu>Ile] | Hb Zara | HBA2:c.274C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34166 |
666 | CD 91 CTT>CCT [Leu>Pro] | Hb Port Phillip | HBA2:c.275T>C | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34167 |
2952 | CD 91 CTT>CGT [Leu>Arg] | Hb La Mancha | HBA2:c.275T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34167 |
2956 | CD 91 CTT>CAT [Leu>His] | Hb Kalavasos | HBA2:c.275T>A | α2 | Causative | α-chain variant | NG_000006.1 | 34167 |
667 | CD 92 CGG>TGG [Arg>Trp] | Hb Cemenelum | HBA1:c.277C>T | HBA2:c.277C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34169, 37973 |
3587 | CD 92 CGG>GGG [Arg>Gly] | Hb Leeuwarden | HBA2:c.277C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34169 |
669 | CD 92 CGG>CTG [Arg>Leu] | Hb Chesapeake | HBA2:c.278G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34170 |
670 | CD 92 CGG>CCG [Arg>Pro] | Hb Monou | HBA2:c.278G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34170 |
673 | CD 94 GAC>TAC [Asp>Tyr] | Hb Setif | HBA2:c.283G>T | α2 | Causative | α-chain variant | NG_000006.1 | 34175 |
674 | CD 94 GAC>AAC [Asp>Asn] | Hb Titusville | HBA2:c.283G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34175 |
675 | CD 94 GAC>CAC [Asp>His] | Hb Sunshine Seth | HBA2:c.283G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34175 |
676 | CD 94 GAC>GTC [Asp>Val] | Hb Kirksey | HBA2:c.284A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34176 |
679 | CD 94 GAC>GAG [Asp>Glu] | Hb Roanne | HBA1:c.285C>G | HBA2:c.285C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34177, 37981 |
680 | CD 95 CCG>GCG [Pro>Ala] | Hb Denmark Hill | HBA2:c.286C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34178 |
682 | CD 95 CCG>TCG [Pro>Ser] | Hb Rampa | NM_000517.4(HBA2):c.286C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34178 |
683 | CD 95 CCG>CTG [Pro>Leu] | Hb G-Georgia | HBA2:c.287C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34179 |
2375 | CD 96 GTC>ATC [Vla>Ile] | Hb El Salvador | HBA2:c.289G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34181 |
686 | CD 96 GTC>GAC [Val>Asp] | Hb El Escorial | HBA2:c.290T>A | α2 | Causative | α-chain variant | NG_000006.1 | 34182 |
687 | CD AAC>CAC [Asn>His] (Hb Shinbashi) | Hb Fuchu-II | HBA2:c.292A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34184 |
2350 | CD 97 AAC>GAC [Asn>Asp] | Hb Cheektowaga | HBA2:c.292A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34184 |
688 | CD 97 AAC>AAA [Asn>Lys] | Hb Dallas | HBA2:c.294C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34186 |
3988 | CD 98 TTC>GTC [Phe>Val] | Hb Xiangzhou | HBA2:c.295T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34187 |
689 | CD 98 TTC>TAC [Phe>Tyr] | Hb Mill Hill | HBA1:c.296T>A | HBA2:c.296T>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34188, 37992 |
2466 | CD 99 AAG>CAG [Lys>Gln] | Hb Burkina Fassa | HBA2:c.298A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34190 |
2416 | CD 99 AAG>ATG [Lys>Met] | N/A | HBA1:c.299A>T | α1 | Causative | α-chain variant | NG_000006.1 | 34191 |
2424 | CD 99 AAG>AGG [Lys>Arg] | Hb Papanui | HBA2:c.299A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34191 |
2370 | CD 99 AAG>AAC [Lys>Asn] | Hb Fulton | HBA2:c.300G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34192 |
692 | CD 102 AGC>CGC [Ser>Arg] | Hb Manitoba I | HBA2:c.307A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34341 |
2304 | CD 102 AGC>AAC (Ser>Asn) | Hb Enschede | HBA2:c.308G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34342 |
694 | CD 102 AGC>AGA [Ser>Arg] | Hb Manitoba III | HBA2:c.309C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34343 |
696 | CD 103 CAC>TAC [His>Tyr] | Hb Lombard | HBA2:c.310C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34344 |
698 | CD 103 CAC>CGC [His>Arg] | Hb Contaldo | HBA1:c.311A>G | HBA2:c.311A>G | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34345, 38156 |
3583 | CD 106 CTG>CGG [Leu>Arg] | Hb Beckett | HBA2:c.320T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34354 |
3913 | CD 107 GTG>CTG [Val>Leu] | Hb Liaobu | HBA2:c.322G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34356 |
2991 | CD 108 ACC>AAC [Thr>Asn] | Hb Rogliano | HBA1:c.326C>A | α1 | Causative | α-chain variant | NG_000006.1 | 34360 |
2571 | CD 109 CTG>CCG [Leu>Pro] | Hb Milano | HBA1:c.329T>C | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34363 |
704 | CD 110 GCC>ACC [Ala>Thr] | Hb Tonosho | HBA1:c.331G>A | HBA2:c.331G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34365, 38176 |
706 | CD 111 GCC>ACC [Ala>Thr] | Hb Mosella | HBA1:c.334G>A | HBA2:c.334G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34368, 38179 |
3982 | CD 111 GCC>TCC [Ala>Ser] | Hb Liuzhou-Yufeng | HBA1:c.334G>T | α1 | Causative | α-chain variant | NG_000006.1 | 34368 |
707 | CD 111 GCC>GTC [Ala>Val] | Hb Anamosa | HBA2:c.335C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34369 |
721 | CD 116-117 +15 bp [+His-Leu-Pro-Ala-Glu] | Hb Zaïre | HBA1:c.337_351dup | HBA2:c.337_351dup | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34371, 38182 |
2360 | CD 112 CAC>TAC [His>Tyr] | Hb Kansas City | HBA2:c.337C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34371 |
2366 | CD 112 CAC>AAC [His>Asn] | Hb Royal Oak | HBA2:c.337C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34371 |
709 | CD 112 CAC>CGC [His>Arg] (Hb Serbia) | Hb Strumica | HBA1:c.338A>G | HBA2:c.338A>G | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34372, 38183 |
3924 | CD 112 CAC>CCC [His>Pro] | Hb Beligneux | HBA2:c.338A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34372 |
3482 | CD 113 CTC>TTC [Leu>Phe] | Hb Pretoria | HBA2:c.340C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34374 |
711 | CD 113 CTC>CGC [Leu>Arg] | Hb San Antonio | HBA2:c.341T>G | α2 | Causative | α-chain variant | NG_000006.1 | 34375 |
712 | CD 113 CTC>CAC [Leu>His] | Hb Twin Peaks | HBA1:c.341T>A | HBA2:c.341T>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34375, 38186 |
713 | CD 114 CCC>TCC [Pro>Ser] | Hb Melusine | NM_000517.6(HBA2):c.343C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34377 |
714 | CD 114 CCC>ACC [Pro>Thr] (Hb Bamako) | Hb Jura | HBA2:c.343C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34377 |
716 | CD 114 CCC>CGC [Pro>Arg] | Hb Chiapas | HBA1:c.344C>G | HBA2:c.344C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34378, 38189 |
2369 | CD 115 -GCC [-Ala] | Hb Towson | HBA2:c.346_348delGCC | α2 | Causative | α-chain variant | NG_000006.1 | 34380 |
717 | CD 115 GCC>GAC [Ala>Asp] | Hb J-Tongariki | HBA1:c.347C>A | HBA2:c.347C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34381, 38192 |
718 | CD 116 GAG>CAG [Glu>Gln] | Hb Oleander | HBA1:c.349G>C | HBA2:c.349G>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34383, 38194 |
3041 | CD 116 GAG>AAG [Glu>Lys] | Hb O-Indonesia | HBA2:c.349G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34383 |
2337 | CD 116 GAG>GTG [Glu>Val] | Hb Walsgrave | HBA2:c.350A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34384 |
722 | CD 117 TTC>ATC [Phe>Ile] | Hb Ambroise Pare | HBA2:c.352T>A | α2 | Causative | α-chain variant | NG_000006.1 | 34386 |
3970 | CD 117 TTC>TTG [Phe>Leu] | Hb Jendouba | HBA2:c.354C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34388 |
3028 | CD 119 CCT>TCT [Pro>Ser] | Hb Macarena | HBA2:c.358C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34392 |
3271 | CD 119 CCT>GCT [Pro>Ala] (Hb Lakeview Terrace) | Hb Arcadia | HBA2:c.358C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34392 |
3716 | CD 119 CCT>CAT [Pro>His] | N/A | HBA2:c.359C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34393 |
727 | CD 120 GCG>GAG [Ala>Glu] (Hb J-Birmingham) | Hb J-Meerut | HBA2:c.362C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34396 |
3029 | CD 121 (+3bp): (+GTG) | Hb El Retiro | HBA2:c.364_366dupGTG | α2 | Causative | α-chain variant | NG_000006.1 | 34398 |
3042 | CD 122 CAC>TAC [His>Tyr] | Hb Yanase | HBA2:c.367C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34401 |
2356 | CD 122 CAC>CTC [His>Leu] | Hb Dubai | HBA2:c.368A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34402 |
730 | CD 122 CAC>CAG [His>Gln] | Hb Westmead | HBA2:c.369C>G | α2 | Causative | α-chain variant | NG_000006.1 | 34403 |
3961 | CD 122/123 (-CG,+GA) | Hb Nanning | HBA2:c.369_370delinsGA | α2 | Causative | α-chain variant | NG_000006.1 | 34403 |
731 | CD 123 GCC>ACC [Ala>Thr] (Hb Croxley Green) | Hb Santa Barnabas | HBA2:c.370G>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34404 |
2457 | CD 123 GCC>GTC [Ala>Val] | Hb Pressath | HBA2:c.371C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34405 |
734 | CD 124 TCC>CCC [Ser>Pro] | Hb Policoro | HBA2:c.373T>C | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34407 |
3748 | CD 124 TCC>ACC [Ser>Thr] | Hb Huadu | HBA2:c.373T>A | α2 | Causative | α-chain variant | NG_000006.1 | 34407 |
2444 | CD 124 TCC>TTC [Ser>Phe] | Hb Batley | HBA1:c.374C>T | HBA2:c.374C>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34408, 38219 |
736 | CD 125 CTG>CAG [Leu>Gln] | Hb West-Einde | HBA2:c.377T>A | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34411 |
3758 | CD 126 GAC>AAC [Asp>Asn] | Hb Tarrant | HBA2:c.379G>A | α2 | Causative | α-chain variant | NG_000006.1 | 34413 |
741 | CD 126 GAC>GGC [Asp>Gly] | Hb West One | HBA2:c.380A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34414 |
742 | CD 126 GAC>GGC [Asp>Val] | Hb Fukutomi | HBA1:c.380A>T | HBA2:c.380A>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34414, 38225 |
2338 | CD 127 AAG>GAG [Lys>Glu] | Hb Coombe Park | HBA2:c.382A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34416 |
744 | CD 127 AAG>ACG [Lys>Thr] | Hb St. Claude | HBA1:c.383A>C | HBA2:c.383A>C | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34417, 38228 |
2530 | CD 127 AAG>AGG [Lys>Arg] | Hb Longview | HBA2:c.383A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34417 |
745 | CD 127 AAG>AAT or AAC [Lys>Asn] | Hb Jackson | HBA1:c.384G>C | HBA1:c.384G>T | HBA2:c.384G>C | HBA2:c.384G>T | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34418, 38229 |
2480 | CD 129 CTG>-TG | Hb Hamilton Hill | HBA2:c.388delC | α2 | Causative | α-chain variant | NG_000006.1 | 34422 |
750 | CD 130 GCT>GAT [Ala>Asp] | Hb Yuda | HBA2:c.392C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34426 |
4085 | CD 132 (+T) | Hb Balkh | HBA2:c.398dup | α2 | Causative | α-chain variant | NG_000006.1 | 34432 |
3404 | CD 133-135 (-AGCACCG) | Hb Aalesund | HBA2:c.400_406del | α2 | Causative | α-chain variant | NG_000006.1 | 34434 |
756 | CD 133 AGC>AAC [Ser>Asn] | Hb Saclay | HBA1:c.401G>A | HBA2:c.401G>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34435, 38246 |
757 | CD 133 AGC>AGA [Ser>Arg] (Hb Footscray) | Hb Val de Marne | HBA2:c.402C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34436 |
758 | CD 134 ACC>GCC [Thr>Ala] | Hb Brunswick | HBA2:c.403A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34437 |
759 | CD 134 ACC>AGC or TCC [Thr>Ser] | Hb Kenton | HBA1:c.403A>T | HBA1:c.404C>G | HBA2:c.403A>T | HBA2:c.404C>G | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34437, 34438, 38248, 38249 |
761 | CD 135 GTG>CTG [Val>Leu] | Hb Tottenham | HBA2:c.406G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34440 |
764 | CD 136 CTG>ATG [Leu>Met] | Hb Chicago | HBA2:c.409C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34443 |
766 | CD 136 CTG>CGG [Leu>Arg] | Hb Toyama | HBA1:c.410T>G | HBA2:c.410T>G | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34444, 38255 |
2540 | CD 137-138 ACCTCC>ACTCTC | Hb Pohnpei | HBA2:c.414_416delinsTCT | α2 | Causative | α-chain variant | NG_000006.1 | 34448 |
768 | CD 138 TCC>CCC [Ser>Pro] | Hb Attleboro | HBA1:c.415T>C | HBA2:c.415T>C | α1 or α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 34449, 38260 |
770 | CD 138 TCC>TTC [Ser>Phe] | Hb Frauenfeld | HBA2:c.416C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34450 |
772 | CD 139 AAA>GAA [Lys>Glu] | Hb Hanamaki-2 | HBA2:c.418A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34452 |
3379 | CD 139 AAA>CAA [Lys>Gln] | Hb Jilin | HBA2:c.418A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34452 |
2981 | CD 139 AAA>AGA [Lys>Arg] | Hb Witham | HBA2:c.419A>G | α2 | Causative | α-chain variant | NG_000006.1 | 34453 |
774 | CD 139 AAA>AAC [Lys>Asn] | Hb Fukui | HBA2:c.420A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34454 |
775 | CD 139 (-A) | Hb Wayne | HBA2:c.420delA | α2 | Causative | α-chain variant | NG_000006.1 | 34454 |
3712 | CD 140 TAC>TCC [Tyr>Ser] | Hb Angers | HBA2:c.422A>C | α2 | Causative | α-chain variant | NG_000006.1 | 34456 |
777 | CD 140 TAC>TAA | Hb Natal | HBA2:c.423C>A | α2 | Causative | α-chain variant | NG_000006.1 | 34457 |
778 | CD 141 CGT>CAT [Arg>Ser] | Hb J-Cubujuqui | HBA1:c.424C>A | HBA2:c.424C>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 34458, 38269 |
780 | CD 141 CTG>TGT [Arg>Cys] | Hb Nunobiki | HBA2:c.424C>T | α2 | Causative | α-chain variant | NG_000006.1 | 34458 |
781 | CD 141 CGT>CCT [Arg>Pro] | Hb Singapore | HBA2:c.425G>C | α2 | Causative | α-chain variant | NG_000006.1 | 34459 |
785 | CD 142 TAA>CAA>CAT | Hb Zurich-Altstetten | HBA2:c.[427T>C;429A>T] | α2 | Causative | α-chain variant | NG_000006.1 | 34461 |
2526 | CD 142 TAA>TTA >172aa | Hb Kinshasa | HBA2:c.428A>T | α2 | Causative | α-chain variant | NG_000006.1 | 34462 |
429 | CD 1 GTG>TTG [Val>Leu] | Hb Baldock | HBA1:c.4G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37583 |
435 | CD 2 CTG>CGG [Leu>Arg] | Hb Chongqing | HBA1:c.8T>G | α1 | Causative | α-chain variant | NG_000006.1 | 37587 |
2352 | CD 2/3 +CTG [+Leu] | Hb Pittsburgh | HBA1:c.9_10insCTG | α1 | Causative | α-chain variant | NG_000006.1 | 37588 |
437 | CD 3 TCT>TTT [Ser>Phe] | Hb Douala | HBA1:c.11C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37590 |
3981 | CD 5 GCC>ACC [Ala>Thr] | Hb Hengqin I | HBA1:c.16G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37595 |
441 | CD 5 GCC>GAC [Ala>Asp] | Hb J-Toronto | HBA1:c.17C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37596 |
442 | CD 6 GAC>TAC [Asp>Tyr] | Hb Woodville | HBA1:c.19G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37598 |
444 | CD 6 GAC>CAC [Asp>His] | Hb Galliera I | HBA1:c.19G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37598 |
3922 | CD 6 GAC>GAG [Asp>Glu] | Hb Brammer | HBA1:c.21C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37600 |
450 | CD 7 AAG>GAG [Lys>Glu] | Hb Kurosaki | HBA1:c.22A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37601 |
2987 | CD 9 AAC>GAC [Asn>Asp] | Hb Farnborough | HBA1:c.28A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37607 |
453 | CD 9 AAC>AGC [Asn>Ser] | Hb Anadour | HBA1:c.29A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37608 |
456 | CD 9 AAC>AAG or AAA [Asn>Lys] | Hb Delfzicht | HBA1:c.30C>G | HBA1:c.30C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37609 |
3953 | CD 11 AAG>CAG [Lys>Gln] | Hb J-Wenchang-Wuming | HBA1:c.34A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37613 |
461 | CD 12 GCC>GAC [Ala>Asp] (Hb J-Aljezur) | Hb J-Paris-I | HBA2:c.38C>A | α2 | Causative | α-chain variant | NG_000006.1 | 37617 |
2386 | CD 13 GCC>ACC [Ala>Thr] | Hb Olivet | HBA1:c.40G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37619 |
2380 | CD 14 TGG>TTG [Trp>Leu] | Hb Basel | HBA1:c.44G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37623 |
465 | CD 15 GGT>CGT [Gly>Arg] (Hb Siam) | Hb Ottawa | HBA1:c.46G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37625 |
2365 | CD 15 GGT>TGT [Gly>Cys] | Hb St. Rose | HBA1:c.46G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37625 |
466 | cd 15 GGT>GAT [Gly>Asp] (Hb J-Oxford , Hb N-Cosenza) | Hb I-Interlaken | HBA1:c.47G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37626 |
2509 | CD 16 AAG>GAG [Lys>Glu] (Hb I-Burlington, Hb I-Philadelphia, Hb I-Skamania, Hb I-Texas) | HbI | HBA1:c.49A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37628 |
468 | CD 16 AAG>ATG [Lys>Met] | Hb Harbin | HBA1:c.50A>T | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37629 |
471 | CD 18 GGC>CGC [Gly>Arg] | Hb Handsworth | HBA1:c.55G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37634 |
2353 | CD 18 GGC>TGC [Gly>Cys] | Hb Lima | HBA1:c.55G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37634 |
3000 | CD 18 GGC>AGC [ Gly>Ser] | Hb King Ecgbert | HBA1:c.55G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37634 |
2285 | CD 20 CAC>CCC [His>Pro] (Hb Anderlecht) | Hb Fulton-Georgia | HBA1:c.62A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37641 |
2317 | CD 20 CAC>CAA [His>Gln] (Hb Le Lamentin) | Hb Brugg | HBA1:c.63C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37642 |
4102 | CD 20 CAC>CAG [His>Gln] | Hb Ormylia | HBA1:c.63C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37642 |
482 | CD 21 GCT>GAT [Ala>Asp] | Hb J-Nyanza | HBA1:c.65C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37644 |
3757 | CD 23 GAG>CAG [Glu>Gln] | Hb Memphis | HBA1:c.70G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37649 |
491 | CD 24 TAT>TGT [Tyr>Cys] | Hb Ramona | HBA1:c.74A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37653 |
3954 | CD 16 AAG>AAC [Lys>Asn] | Hb Beijing | HBA1:c.51G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37656 |
2510 | CD 27 GAG>GAC [Glu>Asp] | Hb Hekinan | HBA1:c.84G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37663 |
2983 | CD 27 GAG>GAT [Glu>Asp] | Hb Hekinan II | HBA1:c.84G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37663 |
2995 | CD 28 GCC>ACC [Ala>Thr] | Hb Bramall Lane | HBA1:c.85G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37664 |
2313 | CD 28 GCC>GTC [Ala>Val] | Hb Nedlands | HBA1:c.86C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37665 |
2310 | CD 29 CTG>GTG [Leu>Val] | Hb Kosovo | HBA1:c.88C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37667 |
502 | CD 30 GAG>CAG [Glu>Gln] (Hb G-Chinese, Hb G-Hong Kong, Hb G-Singapore) | Hb G-Honolulu | NM_000558.5(HBA1):c.91G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37670 |
3767 | CD 30 GAG>AAG [Glu>Lys] | Hb O-Padova | HBA1:c.91G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37670 |
504 | CD 30 GAG>GCG [Glu>Ala] | Hb Bom Jesus da Lapa | HBA1:c.92A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37671 |
505 | CD 30 GAG>GTG [Glu>Val] | Hb Itapira | HBA1:c.92A>T | α1 | Causative | α-chain variant | NG_000006.1 | 37671 |
2402 | CD 31 AGG>ACG [Arg>Thr] | Hb Mao | HBA1:c.95G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37674 |
509 | CD 34 CTG>CGG [Leu>Arg] (Hb Ogi) | Hb Queens | HBA1:c.104T>G | α1 | Causative | α-chain variant | NG_000006.1 | 37800 |
2968 | CD 36 TTC>TAC [ Phe>Tyr] | Hb Kempten | HBA1:c.110T>A | α1 | Causative | α-chain variant | NG_000006.1 | 37806 |
517 | CD 38 ACC>ATC [Thr>Ile] | Hb Chelsea | HBA1:c.116C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37812 |
522 | CD 40 AAG>ACG [Lys>Thr] | Hb Pisa | HBA1:c.122A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37818 |
523 | CD 40 AAG>AAC [Lys>Asn] | Hb Saratoga Springs | HBA1:c.123G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37819 |
2385 | CD 42 TAC>TCC [Tyr>Ser] | Hb Erzeroum | HBA1:c.128A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37824 |
3557 | CD 43 TTC>CTC [Phe>Leu] | Hb Vanvitelli | HBA1:c.130T>C | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37826 |
530 | CD 44 CCG>GCG [Pro>Ala] (Hb Milne) | Hb Hagerstown | HBA1:c.133C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37829 |
3264 | CD 44 CCG>TCG [Pro>Ser] | Hb Wiangpapao | HBA1:c.133C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37829 |
536 | CD 45 CAC>CGC [His>Arg] | Hb Fort de France | HBA1:c.137A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37833 |
542 | CD 47 GAC>AAC [Asp>Asn] | Hb Arya | HBA1:c.142G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37838 |
2500 | CD 47 GAC>CAC [Asp>His] (Hb L-Ferrara, Hb Michigan-I, Hb Michigan-II, Hb Sealy, Hb Sinai) | Hb Hasharon | HBA1:c.142G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37838 |
547 | CD 48 CTG>CCG [Leu>Pro] | Hb Reading | HBA1:c.146T>C | α1 | Causative | α-chain variant | NG_000006.1 | 37842 |
3040 | CD 48 CTG>CGG [Leu>Arg] | Hb Montgomery | HBA1:c.146T>G | α1 | Causative | α-chain variant | NG_000006.1 | 37842 |
3026 | CD 49 AGC>CGC [Ser>Arg] | Hb Puerta del Sol | HBA1:c.148A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37844 |
2993 | CD 49 AGC>AAC [Ser>Asn] | Hb Furuset | HBA1:c.149G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37845 |
2529 | CD 50 +GGAGCC | Hb Bakersfield | HBA1:c.151_152insGGAGCC | α1 | Causative | α-chain variant | NG_000006.1 | 37847 |
550 | CD 50 CAC>CTC [His>Leu] | Hb Dublin | NM_000558.5(HBA1):c.152A>T | α1 | Causative | α-chain variant | NG_000006.1 | 37848 |
2501 | CD 50 CAC>CAG [His>Gln] | Hb Frankfurt | HBA1:c.153C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37849 |
553 | CD 51 GGC>AGC [Gly>Ser] | Hb Riccarton | HBA1:c.154G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37850 |
2502 | CD 51 GGC>CGC [Gly>Arg] | Hb Russ | HBA1:c.154G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37850 |
556 | CD 52-59 (-24 bp) | Hb J-Biskra | HBA1:c.157_180del | α1 | Causative | α-chain variant | NG_000006.1 | 37853 |
3442 | CD 51-58 (+24 bp) | Hb Choisy | HBA1:c.157_180dupTCTGCCCAGGTTAAGGGCCACGGC | α1 | Causative | α-chain variant | NG_000006.1 | 37853 |
3560 | CD 52 TCT>TGT [Ser>Cys] | Hb Dongguan | HBA1:c.158C>G | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37854 |
559 | CD 54 CAG>GAG [Gln>Glu] (Hb J-Paris-II, Hb Uppsala) | Hb Mexico | HBA1:c.163C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37859 |
560 | CD 54 CAG>CGG [Gln>Arg] (Hb Hikoshima) | Hb Shimonoseki | HBA1:c.164A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37860 |
3626 | CD 54 CAG>CAT [Gln>His] | Hb Goole | HBA1:c.165G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37861 |
561 | CD 55 GTT>CTT [Val>Leu] (Hb Poland) | Hb Roubaix | HBA1:c.166G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37862 |
562 | CD 55 GTT>GCT [Val>Ala] (Hb Gerland 1) | Hb Gerland | HBA1:c.167T>C | α1 | Causative | α-chain variant | NG_000006.1 | 37863 |
566 | CD 56 AAG>ACG [Lys>Thr] | Hb Thailand | HBA1:c.170A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37866 |
567 | CD 56 AAG>AAT or AAC [Lys>Asn] | Hb Belliard | HBA1:c.171G>C | HBA1:c.171G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37867 |
568 | CD 57 GGC>CGC [Gly>Arg] | Hb L-Persian Gulf | HBA1:c.172G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37868 |
3075 | CD 56/57 (+24bp) (HBA1:p.Lys57_Gly58insSerHisGlySerAlaGlnValLys , Hb KSVGH) | Hb Kaohsiung Veterans General Hospital | HBA1:c.171_172insAGCCACGGCTCTGCCCAAGTTAGG | α1 | Causative | α-chain variant | NG_000006.1 | 37868 |
3962 | CD 57 GGC>TGC [Gly>Cys] | Hb Kirikiriroa | HBA1:c.172G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37868 |
3175 | CD 58 CAC>CTC [His>Leu] | Hb Kirklareli | HBA1:c.176A>T | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37872 |
573 | CD 59 GGC>AGC [Gly>Ser] | Hb Parma | HBA1:c.178G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37874 |
3624 | CD 60 AAG>GAG [Lys>Glu] | Hb Liuzhou | HBA1:c.182A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37878 |
578 | CD 60 AAG>AAT | Hb Zambia | HBA1:c.183G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37879 |
2982 | CD 61 AAG>AGG [Lys>Arg] | Hb Derby | HBA1:c.185A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37881 |
582 | CD AAG>AAT [Lys>Asn] | Hb J-Buda | HBA1:c.186G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37882 |
3015 | CD 63 GCC>ACC [Ala>Thr] | Hb Greenville-NC | HBA1:c.190G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37886 |
585 | CD 63 GCC>GAC [Ala>Asp] (Hb J-Pontoise) | Hb Pontoise | NM_000558.5(HBA1):c.191C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37887 |
587 | CD 64 GAC>CAC [Asp>His] | Hb Q-India | HBA1:c.193G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37889 |
2528 | CD 64 GAC>AAC [Asp>Asn] (Hb Wädenswil, Hb Burgos) | Hb G-Waimanalo | HBA1:c.193G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37889 |
2455 | CD 64 GAC>GCC [Asp>Ala] | Hb Lucan | HBA1:c.194A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37890 |
594 | CD 68 AAC>CAC [Asn>His] | Hb Jeddah | HBA1:c.205A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37901 |
597 | CD 68 +GCGCTGACCAAC [+Ala-Leu-Thr-Asn] | Hb Esch | HBA1:c.207_208insGCGCTGACCAAC | α1 | Causative | α-chain variant | NG_000006.1 | 37904 |
599 | CD 70 GTG>ATG [Val>Met] | Hb Haaksbergen | HBA1:c.211G>A | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37907 |
2358 | CD 71 GCG>GTG [Ala>Val] (Hb Ozieri) | Hb Allison Park | HBA1:c.215C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37911 |
3312 | CD 72 CAC>CAG [His>Gln] | Hb Madonie | HBA1:c.219C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37915 |
2996 | CD 73 GTG>ATG [Val>Met] | Hb Argenteuil | HBA1:c.220G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37916 |
607 | CD 74 GAC>CAC [Asp>His] (Hb Asabara, Hb G-Taichung, Hb Kurashiki-I, Hb Mahidol) | Hb Q-Thailand | HBA1:c.223G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37919 |
3759 | CD 74 GAC>AAC [Asp>Asn] | Hb G-Pest | HBA1:c.223G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37919 |
608 | CD 74 GAC>GTC [Asp>Val] | Hb Les Lilas | HBA1:c.224A>T | α1 | Causative | α-chain variant | NG_000006.1 | 37920 |
609 | CD 74 GAC>GGC [Asp>Gly] | Hb Chapel Hill | HBA1:c.224A>G | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37920 |
3875 | CD 74 GAC>GAG [Asp>Glu] | Hb Jishui | HBA1:c.225C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37921 |
2503 | CD 75 GAC>TAC [Asp>Tyr] | Hb Winnipeg | HBA1:c.226G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37922 |
3760 | CD 75 GAC>AAC [Asp>Asn] | Hb Matsue-Oki | HBA1:c.226G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37922 |
2485 | CD 77 CCC>TCC [Pro>Ser] | Hb Nile | HBA1:c.232C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37928 |
2504 | CD 77 CCC>CAC [Pro>His] | Hb Toulon | HBA1:c.233C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37929 |
625 | CD 78 AAC>CAC [Asn>His] | Hb Davenport | HBA1:c.235A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37931 |
2505 | CD 78 AAC>AAG [Asn>Lys] | Hb Stanleyville-II | HBA1:c.237C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37933 |
3897 | CD 78 AAC>AAA [Asn>Lys] | Hb Qinzhou | HBA1:c.237C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37933 |
4081 | CD 79 GCG>GTG [Ala>Val] | Hb Tangshan | HBA1:c.239C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37935 |
632 | CD 81 TCC>TGC [Ser>Cys] | Hb Nigeria | HBA1:c.245C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37941 |
633 | CD 82 GCC>ACC (Ala>Thr) | Hb Hagley Park | HBA1:c.247G>A | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37943 |
2281 | CD 83 CTG>CGG [Leu>Arg] | Hb Ahvaz | HBA2: c.251T>G | α2 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37947 |
637 | CD 84 AGC>AGA [Ser>Arg] | Hb Etobicoke | HBA1:c.255C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37949 |
639 | CD 85 GAC>AAC [Asp>Asn] | Hb G-Norfolk | HBA1:c.256G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37952 |
641 | CD 85 GAC>CAC [Asp>His] | Hb Canuts | HBA1:c.256G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37952 |
2336 | CD 86 CTG>GTG [Leu>Val] | N/A | HBA1:c.259C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37955 |
4098 | CD 86 CTG>CCG [Leu>Pro] | Hb Thessaloniki | HBA1:c.260T>C | α1 | Causative | α-chain variant | NG_000006.1 | 37956 |
647 | CD 87 CAC>GAC [His>Asp] | Hb Bonn | HBA1:c.262C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37958 |
2506 | CD 87 CAC>TAC [His>Tyr] (Hb M-Kankakee , Hb M-Oldenburg , Hb M-Sendai) | Hb M-Iwate | HBA1:c.262C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37958 |
649 | CD 87 CAC>CCC [His>Pro] | Hb Grifton | HBA1:c.263A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37959 |
3879 | CD 87 CAC>CTC [His>Leu] | Hb Padma River | HBA1:c.263A>T | α1 | Causative | α-chain variant | NG_000006.1 | 37959 |
3434 | CD 87 CAC>CAG [His>Gln] | Hb Lansing-Ramathibodi | HBA1:c.264C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37960 |
658 | CD 89 CAC>CAG [His>Gln] | Hb Buffalo | HBA1:c.270C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37966 |
662 | CD 90 AAG>AGG [Lys>Arg] | Hb Clinico Madrid II | HBA1:c.272A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37968 |
663 | CD 90 AAG>ACG | Hb J-Rajappen | HBA1:c.272A>C | α1 | Causative | α-chain variant | NG_000006.1 | 37968 |
3756 | CD 90 AAG>AAC [Lys>Asn] | Hb J-Broussais | HBA1:c.273G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37969 |
3993 | CD 90 AAG>AAT [Lys>Asn] | Hb Guigang | HBA1:c.273G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37969 |
665 | CD 91 CTT>TTT [Leu>Phe] (Hb Grey Lynn) | Hb Vientiane | HBA1:c.274C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37970 |
668 | CD 92 CGG>CAG [Arg>Gln] | Hb J-Cape Town | HBA1:c.278G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37973 |
672 | CD 93 GTG>GCG [Val>Ala] | Hb Die | HBA1:c.281T>C | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37977 |
2507 | CD 94 GAC>AAC [Asp>Asn] | Hb Titusville | HBA1:c.283G>A | α1 | Causative | α-chain variant | NG_000006.1 | 37979 |
677 | CD 94 GAC>GCC [Asp>Ala] | Hb Bassett | HBA1:c.284A>C | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 37980 |
678 | CD 94 GAC>GGC [Asp>Gly] | Hb Çapa | HBA1:c.284A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37980 |
681 | CD 95 CCG>ACG [Pro>Thr] | Hb Godavari | NM_000558.3(HBA1):c.286C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37982 |
684 | CD 95 CCG>CGG [Pro>Arg] | Hb St. Luke's | HBA1:c.287C>G | α1 | Causative | α-chain variant | NG_000006.1 | 37983 |
685 | CD 95 CCG>CAG [Pro>Gln] | Hb Wichita | HBA1:c.287C>A | α1 | Causative | α-chain variant | NG_000006.1 | 37983 |
3718 | CD 95 CCG>CTG [Pro>Leu] | Hb Georgia | HBA1:c.287C>T | α1 | Causative | α-chain variant | NG_000006.1 | 37983 |
2357 | CD 96 GTC>CTC [Val>Leu] | Hb Woodstock | HBA1:c.289G>C | α1 | Causative | α-chain variant | NG_000006.1 | 37985 |
3914 | CD 97 AAC>AGC [Asn>Ser] | Hb Northwood | HBA1:c.293A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37989 |
690 | CD 99 AAG>GAG [Lys>Glu] (Hb Turriff-I) | Hb Turriff | NM_000558.5(HBA1):c.298A>G | α1 | Causative | α-chain variant | NG_000006.1 | 37994 |
691 | CD 99 AAG>AAT [Lys>Asn] (Hb Harlow) | Hb Beziers | HBA1:c.300G>T | α1 | Causative | α-chain variant | NG_000006.1 | 37996 |
2303 | CD 100 CTC>TTC (Leu>Phe) | Hb Weesp | HBA1:c.301C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38146 |
2305 | CD 100 CTC>CCC [Leu>Pro] | Hb Corsica | HBA1:c.302T>C | α1 | Causative | α-chain variant | NG_000006.1 | 38147 |
2985 | CD 102 AGC>CGC [Ser>Arg] | Hb Manitoba IV | HBA1:c.307A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38152 |
693 | CD 102 AGC>AGA [Ser>Arg] | Hb Manitoba II | HBA1:c.309C>A | α1 | Causative | α-chain variant | NG_000006.1 | 38154 |
695 | CD 103 CAC>TAC [His>Tyr] | Hb Charolles | HBA1:c.310C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38155 |
2532 | CD 103 CAC>GAC [His>Asp] | Hb Illinois | HBA1:c.310C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38155 |
3956 | CD 104 TGC>TAC [Cys>Tyr] | Hb Sallanches | HBA1:c.314G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38159 |
701 | CD 106 CTG>CCG [Leu>Pro] | Hb Charlieu | HBA1:c.320T>C | α1 | Causative | α-chain variant | NG_000006.1 | 38165 |
2315 | CD 110 GCC>GTC [Ala>Val] (Hb White Rose) | Hb Montluel | HBA1:c.332C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38177 |
708 | CD 112 CAC>GAC [His>Asp] | Hb Hopkins-II | NM_000558.5(HBA1):c.337C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38182 |
2377 | CD 112 CAC>CAA [His>Gln] | Hb West Allis | HBA1:c.339C>A | α1 | Causative | α-chain variant | NG_000006.1 | 38184 |
2316 | CD 114 CCC>GCC [Pro>Ala] | Hb Broomhill | NM_000558.5(HBA1):c.343C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38188 |
715 | CD 114 CCC>CTC [Pro>Leu] | Hb Nouakchott | NM_000558.3(HBA1):c.344C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38189 |
3378 | CD 114 CCC>CAC [Pro>His] | Hb Hubei | HBA1:c.344C>A | α1 | Causative | α-chain variant | NG_000006.1 | 38189 |
2322 | CD 115 GCC>GTC [Ala>Val] | Hb Palmela | HBA1:c.347C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38192 |
720 | CD 116 GAG>AAG [Glu>Lys] (Hb Buginese-X, Hb Oliviere) | Hb O-Indonesia | HBA1:c.349G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38194 |
723 | CD 118-119 +9 bp [+Glu-Phe-Thr] (Hb Dakar) | Hb Grady | HBA1:c.349_357dup | α1 | Causative | α-chain variant | NG_000006.1 | 38194 |
719 | CD 116 GAG>GCG [Glu>Ala] | Hb Ube-4 | HBA1:c.350A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38195 |
3036 | CD 117/118 +TCA [+Ser] | Hb Wexham | HBA1:c.354_355insTCA | α1 | Causative | α-chain variant | NG_000006.1 | 38199 |
726 | CD 119 CCT>CTT [Pro>Leu] | Hb Diamant | HBA1:c.359C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38204 |
2508 | CD 120 GCG>GAG [Ala>Glu] (Hb J-Birmingham) | Hb J-Meerut | HBA1:c.362C>A | α1 | Causative | α-chain variant | NG_000006.1 | 38207 |
728 | CD 121 GTG>ATG [Val>Met] | Hb Owari | HBA1:c.364G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38209 |
729 | CD 122 CAC>TAC [His>Tyr] | Hb Yanase | HBA1:c.367C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38212 |
3751 | CD 122 CAC>GAC [His>Asp] | Hb Daxin | HBA1:c.367C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38212 |
733 | CD 123 GCC>TCC [Ala>Ser] | Hb Mulhacen | HBA1:c.370G>T | α1 | Causative | α-chain variant | NG_000006.1 | 38215 |
3016 | CD 123 GCC>GTC [Ala>Val] | Hb Louisa | HBA1:c.371C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38216 |
2984 | CD124 TCC>TGC [Ser>Cys] | Hb Harehills | HBA1:c.374C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38219 |
2414 | CD 125 CTG>CCG [Leu>Pro] | Hb Quong Sze II | HBA1:c.377T>C | α1 | Causative | α-chain variant | NG_000006.1 | 38222 |
738 | CD 126 GAC>CAC [Asp>His] | Hb Sassari | HBA1:c.379G>C | α1 | Causative | α-chain variant | NG_000006.1 | 38224 |
739 | CD 126 GAC>TΑC [Asp>Tyr] | Hb Montefiore | HBA1:c.379G>T | α1, α1 or α2 | Causative | α-chain variant | NG_000006.1 | 38224 |
2408 | CD 126 GAC>GCC [Asp>Ala] | Hb Verdun | HBA1:c.380A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38225 |
743 | CD 126 GAC>GAG [Asp>Glu] | Hb Burlington | HBA1:c.381C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38226 |
3380 | CD 127 AAG>GAG [Lys>Glu] | Hb Shantou | HBA1:c.382A>G | α1 | Causative | α-chain variant | NG_000006.1 | 38227 |
3789 | CD 127 AAG>CAG [Lys>Gln] | Hb Waikato | HBA1:c.382A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38227 |
749 | CD 130 GCT>GTT [Ala>Val] | Hb Westborough | HBA1:c.392C>T | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 38237 |
752 | CD 131 TCT>TTT | Hb Lusaka | HBA1:c.395C>T | α1 | Causative | α-chain variant | NG_000006.1 | 38240 |
753 | CD 131 TCT>TC- | Hb Fez | HBA1:c.396delT | α1 | Causative | α-chain variant | NG_000006.1 | 38241 |
2323 | CD 132 GTG>ATG [Val>Met] | Hb Portimão | HBA1:c.397G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38242 |
3723 | CD 132 GTG>GCG [Val>Ala] | N/A | HBA1:c.398T>C | α1 | Causative | α-chain variant | NG_000006.1 | 38243 |
4027 | CD 133 AGC>CGC [Ser>Arg] | Hb Val de Marne | HBA2:c.400A>C | α2 | Causative | α-chain variant | NG_000006.1 | 38245 |
760 | CD 134 -C | Hb Senlis | HBA1:c.404delC | α1 | Causative | α-chain variant, Haemolytic anaemia | NG_000006.1 | 38249 |
762 | CD 135 GTG>CTG [Val>Met] | Hb Trenton | HBA1:c.406G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38251 |
763 | CD 135 GTG>ATG [Val>Glu] | Hb Pavie | HBA1:c.407T>A | HBA2:c.407T>A | α1 or α2 | Causative | α-chain variant | NG_000006.1 | 38252 |
3724 | CD 136 CTG>CAG [Leu>Gln] | N/A | HBA1:c.410T>A | α1 | Causative | α-chain variant | NG_000006.1 | 38255 |
767 | CD 137 ACC>CCC [Thr>Pro] | Hb Verona | HBA1:c.412A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38257 |
3802 | CD 138 TCC>GCC [Ser>Ala] | Hb Paynesville | HBA1:c.415T>G | α1 | Causative | α-chain variant | NG_000006.1 | 38260 |
769 | CD 138 TCC>TGC [Ser>Cys] | Hb Ecuador | HBA1:c.416C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38261 |
771 | CD 139 AAA>GAA [Ala>Glu] | Hb Hanamaki-1 | HBA1:c.418A>G | α1 | Causative | α-chain variant | NG_000006.1 | 38263 |
4017 | CD 139 AAA>TAA [Lys>STOP] (Tenerife) | Hb Nivaria | HBA1:c.418A>T | α1 | Causative | α-chain variant | NG_000006.1 | 38263 |
773 | CD 139 AAA>ACA [Lys>Thr] | Hb Tokoname | NM_000558.5(HBA1):c.419A>C | α1 | Causative | α-chain variant | NG_000006.1 | 38264 |
776 | CD 140 TAC>CAC [Tyr>His] | Hb Ethiopia | NM_000558.5(HBA1):c.421T>C | α1 | Causative | α-chain variant | NG_000006.1 | 38266 |
3972 | CD 140 TAC>TAA [Tyr>STOP] | Hb Natal | HBA1:c.423C>A | α1 | Causative | α-chain variant | NG_000006.1 | 38268 |
779 | CD 141 CGT>GGT [Arg>Gly] | Hb J-Camagüey | NM_000558.3(HBA1):c.424C>G | α1 | Causative | α-chain variant | NG_000006.1 | 38269 |
782 | CD 141 CGT>CTT [Arg>Leu] | Hb Legnano | HBA1:c.425G>T | α1 | Causative | α-chain variant | NG_000006.1 | 38270 |
783 | CD 141 CGT>CAT [Arg>His] | Hb Suresnes | NM_000558.3(HBA1):c.425G>A | α1 | Causative | α-chain variant | NG_000006.1 | 38270 |
3890 | CD 18 GGC>TGC [Gly>Cys] | Hb Jiujiang | HBA2:c.55G>T | α2 | Causative | α-chain variant | NG_000006.1 | 172967 |
1404 | (Hb Anti-Lepore Hong Kong) | Hb Hong Kong | NG_000007.3:g.63160_70572dup | δ, β | Causative | δ-chain variant | NG_000007.3 | |
1405 | (Hb Anti-Lepore P-Nilotic) | Hb P-Nilotic | NG_000007.3:g.63461_70874dup | δ, β | Causative | δ-chain variant | NG_000007.3 | |
2378 | CD 6 GAG>CAG [Glu>Gln] | Hb A2-Ramallah | HBD:c.19G>C | δ | Causative | δ-chain variant | NG_000007.3 | 0 |
3390 | βδβ hybrid | Hb Palencia | N/A | δ, β | Causative | β-chain variant | NG_000007.3 | 0 |
1406 | CD 1 GGT>TGT | Hb F-Malaysia | HBG2:c.4G>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 42891 |
2449 | CD 1 GGT>AGT [Gly>Ser] | Hb F-Montchat | HBG2:c.4G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42891 |
3319 | CD 1 GGT>GAT [Gly>Asp] | Hb F-Hayward | HBG2:c.5G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42892 |
1407 | CD 5 GAG>GGG | Hb F-Meinohama | HBG2:c.17A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 42904 |
1409 | CD 7 GAC>AAC | Hb F-Auckland | HBG2:c.22G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42909 |
1410 | CD 8 AAG>CAG or GAG | Hb F-Albaicin | HBG2:c.25A>C | HBG2:c.25A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 42912 |
1412 | CD 12 ACA>AGA [Thr>Arg] | Hb F-Heather | HBG2:c.38C>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 42925 |
3804 | CD 13 AGC>AGA [Ser>Arg] | Hb F-Millennium Park | HBG2:c.42C>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42929 |
1413 | CD 15 TGG>CGG | Hb F-Catalonia | HBG2:c.46T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 42933 |
1414 | CD 16 GGC>CGC | Hb F-Melbourne | HBG2:c.49G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 42936 |
1415 | CD 17 AAG>AAC or AAT | Hb F-Clamart | HBG2:c.54G>C | HBG2:c.54G>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 42941 |
2149 | N/A (Hb Gγ-β Ulsan) | Hb Ulsan | NG_000007.3:g.42946_70654del | Aγ, Gγ, δ, β, pseudo β | Causative | β-chain variant | NG_000007.3 | 42946 |
1416 | CD 19 AAT>AAA or AAG | Hb F-Ouled Rabah | HBG2:c.60T>A | HBG2:c.60T>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 42947 |
1417 | CD 20 GTG>GCG | Hb F-Bron | HBG2:c.62T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 42949 |
1418 | CD 21 GAA>AAA | Hb F-Saskatoon | HBG2:c.64G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42951 |
1419 | CD 21 GAA>CAA | Hb F-Fuchu | HBG2:c.64G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 42951 |
4099 | CD 22 GAT>CAT [Asp>His] | Hb F-Nancy | HBG2:c.67G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 42954 |
1420 | CD 22 GAT>GTT | Hb F-Granada | HBG2:c.68A>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 42955 |
1421 | CD 22 GAT>GGT | Hb F-Urumqi | HBG2:c.68A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 42955 |
3566 | CD 24 GGA>GAA [Gly>Glu] | Hb F-Wentzville | HBG2:c.74G>A | Gγ | Causative | γ-chain variant, Haemolytic anaemia | NG_000007.3 | 42961 |
1422 | CD 25 GGA>GAA | Hb F-Cosenza | HBG2:c.77G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42964 |
1423 | CD 26 GAA>AAA | Hb F-Oakland | HBG2:c.79G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42966 |
3322 | CD 28 CTG>ATG [Leu>Met] | Hb F-M Viseu | HBG2:c.85C>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 42972 |
1424 | CD 34 GTC>ATC | Hb F-Tokyo | HBG2:c.103G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43112 |
2428 | CD 37 TGG>GGG [Trp>Gly] | Hb F-Cobb II | HBG2:c.112T>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43121 |
1425 | CD 38 ACC>CCC | Hb F-Bonheiden | HBG2:c.115A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43124 |
1426 | CD 40 AGG>GGG | Hb F-Veleta | HBG2:c.121A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43130 |
1427 | CD 40 AGG>AAG | Hb F-Austell | HBG2:c.122G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43131 |
2427 | CD 41 TTC>CTC [Phe>Leu] | Hb F-Avellino | HBG2:c.124T>C | Gγ | Causative | γ-chain variant, Hb F levels | NG_000007.3 | 43133 |
1428 | CD 41 TTC>TCC | Hb F-Cincinnati | HBG2:c.125T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43134 |
1429 | CD 44 AGC>CGC | Hb F-Lodz | HBG2:c.133A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43142 |
3608 | CD 50 (TCT>TGT);CD 75(ATA>ACA) | Hb F-Madrid | HBG2:c.[152C>G;227T>C] | Gγ | Causative | γ-chain variant | NG_000007.3 | 43161 |
1430 | CD 55 ATG>AGG | Hb F-Kingston | HBG2:c.167T>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43176 |
1431 | CD 59 AAA>CAA | Hb F-Sacromonte | HBG2:c.178A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43187 |
1432 | CD 59 AAA>GAA | Hb F-Emirates | HBG2:c.178A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43187 |
2552 | CD 59 AAA>AGA [Lys>Arg] | Hb F-Augusta GA | HBG2:c.179A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43188 |
1433 | CD 63 CAT>TAT | Hb F-M-Osaka | HBG2:c.190C>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 43199 |
3369 | CD 63 CAT>CTT [His>Leu] | Hb F-Circleville | HBG2:c.191A>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 43200 |
2471 | CD 64 GGC>GAC [Gly>Asp] | Hb F-Turritana | HBG2:c.194G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43203 |
1434 | CD 65 AAG>AAT or AAC | Hb F-Clarke | HBG2:c.198G>C | HBG2:c.198G>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 43207 |
1435 | CD 66 AAG>CAG | Hb F-Brooklyn | HBG2:c.199A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43208 |
1436 | CD 66 AAG>AGG | Hb F-Shanghai | HBG2:c.200A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43209 |
2435 | CD 67 GTG>ATG [Val>Met] (Hb F-Heuried) | Hb Toms River | HBG2:c.202G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43211 |
1437 | CD 72 GGA>CGA | Hb F-Minoo | HBG2:c.217G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43226 |
1438 | CD 73 GAT>GCT | Hb F-Joanopolis | HBG2:c.221A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43230 |
1439 | CD 75 ATA>GTA | Hb F-Coigneres | HBG2:c.226A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43235 |
1440 | CD 75 ATA>ACA | Hb F-Lesvos | HBG2:c.227T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43236 |
1441 | CD 77 CAC>CGC | Hb F-Kennestone | HBG2:c.233A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43242 |
1442 | CD 79 GAT>CAT [Asp>His] | Hb F-Saint-Etienne | HBG2:c.238G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43247 |
3803 | CD 79 GAT>GGT [Asp>Gly] | Hb F-Northerly Island | HBG2:c.239A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43248 |
1443 | CD 80 GAT>AAT | Hb F-Marietta | HBG2:c.241G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43250 |
1444 | CD 80 GAT>TAT [Asp>Tyr] | Hb F-Paulinia | HBG2:c.241G>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 43250 |
3389 | CD 89 AGT>AAT [Ser>Asn] | Hb F-Careggi | HBG2:c.269G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43278 |
1445 | CD 92 CAC>TAC | Hb F-M-Fort Ripley | HBG2:c.277C>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 43286 |
2395 | CD 93 TGT>CGT [Cys>Arg] | Hb F-Monserrato-Sassari | HBG2:c.280T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43289 |
1446 | CD 94 GAC>AAC | Hb F-Columbus-GA | HBG2:c.283G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43292 |
1447 | CD 97 CAT>CGT [His>Arg] | Hb F-Lyon | HBG2:c.293A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 43302 |
1448 | CD 101 GAG>CAG [Glu>Gln] | Hb F-Zheijang | HBG2:c.304G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43313 |
1449 | CD 101 GAG>AAG | Hb F-La Grange | HBG2:c.304G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43313 |
1450 | CD 102 AAC>ACC [Asn>Thr] | Hb F-Sarajevo | HBG2:c.308A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43317 |
1451 | CD 104 AAG>AAC | Hb F-Macedonia-II | HBG2:c.315G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 43324 |
2459 | CD 105 CTC>CAC [Leu>His] | Hb F-Brugine/Feldkirch | HBG2:c.317T>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 43326 |
1452 | CD 108 AAT>AAA [Asn>Lys] | Hb F-Ube | HBG1:c.327T>A | HBG2:c.327T>A | Aγ or Gγ | Causative | γ-chain variant | NG_000007.3 | 44222, 49140 |
1453 | CD 117 CAT>CGT | Hb F-Malta-I | HBG2:c.353A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 44248 |
1454 | CD 118 TTC>CTC | Hb F-Calabria | HBG2:c.355T>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 44250 |
3891 | CD 119 GGC>CGC [Gly>Arg] | Hb F-Pill Hill | HBG2:c.358G>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 44253 |
1455 | CD 120 AAA>CAA | Hb F-Caltech | HBG2:c.361A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 44256 |
1456 | CD 121 GAA>AAA | Hb F-Carlton | HBG2:c.364G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 44259 |
1457 | CD 125 GAG>GCG | Hb F-Port Royal | HBG2:c.377A>C | Gγ | Causative | γ-chain variant | NG_000007.3 | 44272 |
1458 | CD 130 TGG>GGG | Hb F-Poole | HBG2:c.391T>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 44286 |
2450 | CD 136 GGA>GAA [Gly>Glu] | Hb F-Privas | HBG2:c.410G>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 44305 |
3950 | CD 140 GCC>GAC [Ala>Asp] | Hb F-Wyandotte | HBG2:c.422C>A | Gγ | Causative | γ-chain variant | NG_000007.3 | 44317 |
1459 | CD 146 CAC>TAC | Hb F-Onoda | HBG2:c.439C>T | Gγ | Causative | γ-chain variant | NG_000007.3 | 44334 |
2394 | CD 146 CAC>CGC [His>Arg] | Hb F-Istambul | HBG2:c.440A>G | Gγ | Causative | γ-chain variant | NG_000007.3 | 44335 |
1460 | CD 2 CAT>CAG | Hb F-Macedonia-I | HBG1:c.9T>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 47820 |
1461 | CD 5 GAG>AAG | Hb F-Texas-I | HBG1:c.16G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 47827 |
1408 | CD 6 GAG>AAG | Hb F-Texas-II | HBG1:c.19G>A | HBG2:c.19G>A | Aγ or Gγ | Causative | γ-chain variant | NG_000007.3 | 47830 |
1462 | CD 6 GAG>CAG | Hb F-Pordenone | HBG1:c.19G>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 47830 |
1463 | CD 6 GAG>GGG | Hb F-Kotobuki | HBG1:c.20A>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 47831 |
1411 | CD 12 ACA>AAA [Thr>Lys] | Hb F-Alexandra | HBG1:c.38C>A | HBG2:c.38C>A | Aγ or Gγ | Causative | γ-chain variant | NG_000007.3 | 47849 |
1464 | CD 12 ACA>AGA | Hb F-Calluna | HBG1:c.38C>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 47849 |
3320 | CD 16 GGC>GAC [Gly>Asp] | Hb F-Chori-I | HBG1:c.50G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 47861 |
1465 | CD 22 GAT>AAT [Asp>Asn] | Hb F-Beni Khirane | HBG1:c.67G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 47878 |
1466 | CD 22 GAT>GGT | Hb F-Kuala Lumpur | HBG1:c.68A>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 47879 |
1467 | CD 23 (-GCT) | Hb F-Mauritius | HBG1:c.70_72del | Aγ | Causative | γ-chain variant | NG_000007.3 | 47881 |
1468 | CD 25 GGA>CGA | Hb F-Xinjiang | HBG1:c.76G>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 47887 |
3321 | CD 29 GGA>GAA [Gly>Glu] | Hb F-Chori-II | HBG1:c.89G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 47900 |
1469 | CD 36 CCA>CGA | Hb F-Pendergrass | HBG1:c.110C>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48043 |
1470 | CD 37 TGG>GGG | Hb F-Cobb | HBG1:c.112T>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48045 |
1471 | CD 39 CAG>CGG | Hb F-Bonaire-GA | HBG1:c.119A>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48052 |
1472 | CD 40 AGG>AAG | Hb F-Woodstock | HBG1:c.122G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48055 |
1473 | CD 43 GAC>AAC | Hb F-Fukuyama | HBG1:c.130G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48063 |
1474 | CD 53 GCC>GAC | Hb F-Beech Island | HBG1:c.161C>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48094 |
1475 | CD 61 AAG>GAG | Hb F-Jamaica | HBG1:c.184A>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48117 |
3917 | CD 67 GTG>ATG [Val>Met] | Hb Toms River | HBG1:c.202G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48135 |
1476 | CD 72 GGA>CGA | Hb F-Iwata | HBG1:c.217G>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 48150 |
1477 | CD 73 GAT>CAT | Hb F-Xin-Su | HBG1:c.220G>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 48153 |
1478 | CD 73 GAT>AAT | Hb F-Forest Park | HBG1:c.220G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48153 |
1479 | CD 75 ATA>ACA | Hb F-Sardinia (AgammaT) | HBG1:c.227T>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 48160 |
1480 | CD 79 GAT>AAT | Hb F-Dammam | HBG1:c.238G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48171 |
1481 | CD 80 GAT>AAT | Hb F-Yamaguchi | HBG1:c.241G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 48174 |
1482 | CD 80 GAT>TAT [Asp>Tyr] | Hb F-Victoria Jubilee | HBG1:c.241G>T | Aγ | Causative | γ-chain variant | NG_000007.3 | 48174 |
1498 | (HPFH-7, Kenya) | Hb Kenya | NG_000007.3:g.48194_70985del | Aγ, δ, β, pseudo β | Causative | β-chain variant, Hb F levels | NG_000007.3 | 48194 |
2415 | CD 91 CTG>CGG [Leu>Arg] | Hb F-Moyen-Orient | HBG1:c.275T>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48208 |
1483 | CD 97 CAT>CGT | Hb F-Dickinson | HBG1:c.293A>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 48226 |
2556 | CD 113 GTT>ATT [Val>Ile] | Hb F-Sykesville MD | HBG1:c.340G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 49153 |
1484 | CD 119 GGC>AGC [Gly>Ser] | Hb F-Osilo | HBG1:c.358G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 49171 |
1485 | CD 121 GAA>AAA [Glu>Lys] (Hb F-Siena) | Hb F-Hull | HBG1:c.364G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 49177 |
1487 | CD 121 GAA>CAA | Hb F-Campinas | HBG1:c.364G>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 49177 |
2396 | CD 121 GAA>GTA [Glu>Val] | Hb F-Salamanque | HBG1:c.365A>T | Aγ | Causative | γ-chain variant | NG_000007.3 | 49178 |
2453 | CD 125 GAG>GCG [Glu>Ala] | Hb F-Port Royal II | HBG1:c.377A>C | Aγ | Causative | γ-chain variant | NG_000007.3 | 49190 |
1488 | CD 128 GCT>ACT | Hb F-Baskent | HBG1:c.385G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 49198 |
1489 | CD 131 CAG>CAT [Gln>His] | Hb F-Oman | HBG1:c.396G>T | Aγ | Causative | γ-chain variant | NG_000007.3 | 49209 |
1490 | CD 134 GTG>ATG | Hb F-Jiangsu | HBG1:c.403G>A | Aγ | Causative | γ-chain variant | NG_000007.3 | 49216 |
1491 | CD 136 GCA>TCA | Hb F-Porto Torres | HBG1:c.409G>T | Aγ | Causative | γ-chain variant | NG_000007.3 | 49222 |
1492 | CD 136 GCA>GGA | Hb F-Charlotte | HBG1:c.410C>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 49223 |
3892 | CD 139 AGT>AGG [Ser>Arg] | Hb F-Streeterville | HBG1:c.420T>G | Aγ | Causative | γ-chain variant | NG_000007.3 | 49233 |
4096 | Hb Anti-Lepore Laibin | Hb Anti-Lepore Laibin | NG_000007.3:g.63100_70511dup | δ, β | Causative | δ-chain variant | NG_000007.3 | 63100 |
3964 | Hb Anti-Lepore Liuzhou | N/A | NG_000007.3:g.63154_70565dup | δ, β | Causative | δ-chain variant | NG_000007.3 | 63154 |
1347 | CD 1 GTG>GCG | Hb A2-Niigata | HBD:c.5T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63187 |
2328 | CD 2 CAT>AAT [His>Asn] | Hb A2-Calderdale | HBD:c.7C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63189 |
1348 | CD 2 CAT>CTT | Hb A2-Catania | HBD:c.8A>T | δ | Causative | δ-chain variant | NG_000007.3 | 63190 |
1349 | CD 2 CAT>CGT | Hb A2-Sphakiá | HBD:c.8A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63190 |
3366 | CD 3 CTG>CCG [Leu>Pro] | Hb A2-Sile | HBD:c.11T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63193 |
1350 | CD 4 ACT>AGT [Thr>Ser] | Hb A2-Acacias | HBD:c.14C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63196 |
4035 | CD 7 GAG>AAG [Glu>Lys] | Hb A2-Zhengzhou | HBD:c.22G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63204 |
1351 | CD 7 GAG>GCG [Glu>Ala] | Hb A2-Udine | HBD:c.23A>C | δ | Causative | δ-chain variant | NG_000007.3 | 63205 |
2325 | CD 7 GAG>GAC [Glu>Asp] | Hb A2-Pordenone | HBD:c.24G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63206 |
1352 | CD 8 AAG>GAG [Lys>Glu] | Hb A2-Toranomon | HBD:c.25A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63207 |
4030 | CD 8 AAG>AAC [Lys>Asn] | Hb A2-Hengyang | HBD:c.27G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63209 |
3243 | CD 10 GCT>CCT [Ala>Pro] | Hb A2-Guangzhou | HBD:c.31G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63213 |
3496 | CD 10 GCT>GTT [Ala>Val] | Hb A2-Canakkale | HBD:c.32C>T | δ | Causative | δ-chain variant | NG_000007.3 | 63214 |
1353 | CD 11 GTC>GGC | Hb A2-Pylos | HBD:c.35T>G | δ | Causative | δ-chain variant | NG_000007.3 | 63217 |
2299 | CD 12 AAT>ACT (Asn>Thr) | Hb A2-Rotterdam | HBD:c.38A>C | δ | Causative | δ-chain variant | NG_000007.3 | 63220 |
1354 | CD 12 AAT>AAA [Asn>Lys] | Hb A2-NYU | HBD:c.39T>A | δ | Causative | δ-chain variant | NG_000007.3 | 63221 |
1355 | CD 13 GCC>GAC [Ala>Asp] (Hb A2-Corleone) | Hb A2-MUMC | HBD:c.41C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63223 |
3628 | CD 15 TGG>CGG [Trp>Arg] | Hb A2-Utah | HBD:c.46T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63228 |
3372 | CD 15 TGG>TTG [Trp>Leu] | Hb A2-Stockholm | HBD:c.47G>T | δ | Causative | δ-chain variant | NG_000007.3 | 63229 |
1356 | CD 16 GGC>CGC | Hb A2' or Hb B2 | HBD:c.49G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63231 |
3242 | CD 17 AAA>ACA [Lys>Thr] | Hb A2-Qingyuan | HBD:c.53A>C | δ | Causative | δ-chain variant | NG_000007.3 | 63235 |
4039 | CD 18 GTG>GGG [Val>Gly] | Hb A2-Siping | HBD:c.56T>G | δ | Causative | δ-chain variant | NG_000007.3 | 63238 |
1357 | CD 20 GTG>GAG | Hb A2-Roosevelt | HBD:c.62T>A | δ | Causative | δ-chain variant | NG_000007.3 | 63244 |
3241 | CD 21 GAT>GGT [Asp>Gly] | Hb A2-Dongguan | HBD:c.65A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63247 |
1396 | (δβδ hybrid) | Hb Parchman | NG_000007.3:g.[63249_70661del;63571_70985dup] | δ, β | Causative | δ-chain variant | NG_000007.3 | 63249 |
1401 | (Hb Anti-Lepore Miyada) | Hb Miyada | NG_000007.3:g.63249_70661dup | δ, β | Causative | N/A | NG_000007.3 | 63249 |
2447 | CD 22 GCA>ACA>AAA [Ala>Lys] | Hb A2-Marseille | HBD:c.[67G>A; 68C>A] | δ | Causative | δ-chain variant | NG_000007.3 | 63249 |
1358 | CD 22 GCA>GAA [Ala>Glu] | Hb A2-Flatbush | HBD:c.68C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63250 |
1359 | CD 24 GGT>GAT | Hb A2-Victoria | HBD:c.74G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63256 |
1360 | CD 25 GGT>GAT | Hb A2-Yokoshima | HBD:c.77G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63259 |
1361 | CD 26 GAG>GAC | Hb A2-Puglia | HBD:c.81G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63263 |
3240 | CD 28 CTG>CCG [Leu>Pro] | Hb A2-Hunan | HBD:c.86T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63268 |
2437 | CD 29 GGC>GAC [Gly>Asp] | Hb A2-Hong Kong | HBD:c.89G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63271 |
1363 | CD 36 CCT>CAT | Hb A2-Metaponto | HBD:c.110C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63420 |
3387 | CD 36 CCT>CGT [Pro>Arg] | Hb A2-Sanremo | HBD:c.110C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63420 |
4029 | CD 39 CAG>AAG [Gln>Lys] | Hb A2-Chengdu | HBD:c.118C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63428 |
2320 | CD 39 CAG>CAC [Gln>His] | Hb A2-Lyon | HBD:c.120G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63430 |
4037 | CD 40 AGG>AGT [Arg>Ser] | Hb A2-Wuhan | HBD:c.123G>T | δ | Causative | δ-chain variant | NG_000007.3 | 63433 |
1364 | CD 43 GAG>AAG | Hb A2-Melbourne | HBD:c.130G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63440 |
1365 | CD 43 GAG>GGG | Hb A2-Agrinio | HBD:c.131A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63441 |
4069 | CD 46 GGG>AGG [Gly>Arg] | Hb A2-Yulin | HBD:c.139G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63449 |
2425 | CD 46 GGG>GAG [Gly>Glu] | Hb A2-Tunis | HBD:c.140G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63450 |
3317 | CD 47 GAT>AAT [Asp>Asn] | Hb A2-Lampang | HBD:c.142G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63452 |
1366 | CD 47 GAT>GTT | Hb A2-Parkville | HBD:c.143A>T | δ | Causative | δ-chain variant | NG_000007.3 | 63453 |
2426 | CD 50 TCT>ACT [Ser>Thr] | Hb A2-Konz | HBD:c.151T>A | δ | Causative | δ-chain variant | NG_000007.3 | 63461 |
1367 | CD 51 CCT>CGT | Hb A2-Adria | HBD:c.155C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63465 |
2329 | CD 52 GAT>CAT [Asp>His] | Hb A2-Walsgrave | HBD:c.157G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63467 |
3316 | CD 53 GCT>CCT [Ala>Pro] | Hb A2-Edirne | HBD:c.160G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63470 |
3315 | CD 56 GGC>GAC [Gly>Asp] | Hb A2-Shah Alam | HBD:c.170G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63480 |
1368 | CD 57 AAC>AAA | Hb A2-Campania | HBD:c.174C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63484 |
1369 | CD 59 AAG>ATG [Lys>Met] | Hb A2-North Africa | HBD:c.179A>T | δ | Causative | δ-chain variant | NG_000007.3 | 63489 |
1370 | CD 59 AAG>AAC | Hb A2-Pasteur-Tunis | HBD:c.180G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63490 |
1371 | CD 64 GGC>AGC (Gly>Ser) (Hb A2-Venlo) | Hb A2-Fogo | HBD:c.193G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63503 |
4036 | CD 65 AAG>ATG [Lys>Met] | Hb A2-Zhaoqing | HBD:c.197A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63507 |
3495 | CD 65 AAG>AAT [Lys>Asn] | Hb A2-Yunnan | HBD:c.198G>T | δ | Causative | δ-chain variant | NG_000007.3 | 63508 |
1372 | CD 69 GGT>CGT | Hb A2-Indonesia | HBD:c.208G>C | δ | Causative | δ-chain variant | NG_000007.3 | 63518 |
3406 | CD 69 GGT>GAT [Gly>Asp] | Hb A2-Gebenstorf | HBD:c.209G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63519 |
1373 | CD 70 GCC>GGC [Ala>Gly] (Cubstitution of Ala with Gly at helical position E14, which is in contact with heme.) | Hb A2-Ventimiglia | HBD:c.212C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63522 |
3335 | CD 73 GAT>GTT [Asp>Val] | Hb A2-Henan | HBD:c.221A>T | δ | Causative | δ-chain variant | NG_000007.3 | 63531 |
2324 | CD 74 GGC>GAC [Gly>Asp] | Hb A2-Asti | HBD:c.224G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63534 |
1374 | CD 75 CTG>GTG | Hb A2-Grovetown | HBD:c.226C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63536 |
4092 | CD 76 GCT>GAT [Ala>Asp] | Hb A2-Moyen-Orient | HBD:c.230C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63540 |
3256 | CD 77 CAC>CGC [His>Arg] | Hb A2-Kiriwong | HBD:c.233A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63543 |
4091 | CD 79 GAC>AAC [Asp>Asn] | Hb A2-Guangxi | HBD:c.238G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63548 |
2477 | CD 79 GAC>GGC [Asp>Gly] | Hb A2-Turkish | HBD:c.239A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63549 |
4032 | CD 80 AAC>AAA [Asn>Lys] | Hb A2-Lishui | HBD:c.243C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63552 |
2309 | CD 81 CTC>TTC [Leu>Phe] (Hb A2-Saint-Denis) | Hb A2-St. George's | HBD:c.244C>T | δ | Causative | δ-chain variant | NG_000007.3 | 63554 |
3992 | CD 82 AAG>AAT [Lys>Asn]; CD133 GTG>ATG [Val>Met] | Hb A2-Roi-Et | HBD:c.[249G>T;400G>A] | δ | Causative | δ-chain variant | NG_000007.3 | 63559, 64608 |
1375 | CD 83 GGC>GAC [Gly>Asp] | Hb A2-Nishishinbashi | HBD:c.251G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63561 |
1376 | CD 85 TTT>TCT | Hb A2-Etolia | HBD:c.257T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63567 |
1377 | CD 87 CAG>AAG | Hb A2-Montechiaro | HBD:c.262C>A | δ | Causative | δ-chain variant | NG_000007.3 | 63572 |
4016 | CD 87 CAG>CGG [Gln>Arg] | Hb A2-Cremona | HBD:c.263A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63573 |
1378 | CD 88 CTG>GTG | Hb A2-Lucania | HBD:c.265C>G | δ | Causative | δ-chain variant | NG_000007.3 | 63575 |
3547 | CD 89 AGT>AAT [Ser>Asn] | Hb A2-Pistoia | HBD:c.269G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63579 |
2476 | CD 90 GAG>AAG [Glu>Lys] | Hb A2-Canebière | HBD:c.271G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63581 |
1379 | CD 90 GAG>GTG [Glu>Val] | Hb A2-Honai | HBD:c.272A>T | δ | Causative | δ-chain variant | NG_000007.3 | 63582 |
2354 | CD 90 GAG>GGG [Glu>Gly] | Hb A2-India | HBD:c.272A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63582 |
3383 | CD 91 CTG>CCG [Leu>Pro] | Hb A2-Courbevoie | HBD:c.275T>C | δ | Causative | δ-chain variant | NG_000007.3 | 63585 |
1380 | CD 93 TGT>GGT | Hb A2-Sant' Antioco | HBD:c.280T>G | δ | Causative | δ-chain variant | NG_000007.3 | 63590 |
4013 | CD 93 TGT>TGG [Cys>Trp] | Hb A2-Pontedera | HBD:c.282T>G | δ | Causative | δ-chain variant | NG_000007.3 | 63592 |
4031 | CD 96 CTG>CGG [Leu>Arg] | Hb A2-Hubei | HBD:C.290T>G | δ | Causative | δ-chain variant | NG_000007.3 | 63600 |
3222 | CD 97 CAC>CGC [His>Arg] | Hb A2-Merchang | HBD:c.293A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63603 |
1382 | CD 99 GAT>AAT | Hb A2-Canada | HBD:c.298G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63608 |
4038 | CD 99 GAT>GGT [Asp>Gly] | Hb A2-Wanxian | HBD:c.299A>G | δ | Causative | δ-chain variant | NG_000007.3 | 63609 |
3003 | CD 100 CCT>TCT [Pro>Ser] | Hb A2-Saurashtra | HBD:c.301C>T | δ | Causative | δ-chain variant | NG_000007.3 | 63611 |
3002 | CD 104 AGG>AAG [Arg>Lys] | Hb Chori-Burnaby | HBD:c.314G>A | δ | Causative | δ-chain variant | NG_000007.3 | 63624 |
1383 | CD 104 AGG>AGT | Hb A2-Capri | HBD:c.315G>T | δ | Causative | δ-chain variant | NG_000007.3 | 63625 |
1403 | (Hb Anti-Lepore P-India) | Hb P-India | NG_000007.3:g.63632_71046dup | δ, β | Causative | δ-chain variant | NG_000007.3 | 63632 |
2201 | CD 107 G>A [Gly>Asp] | Hb A2-Tianhe | HBD:c.323G>A | δ | Causative | δ-chain variant | NG_000007.3 | 64531 |
3235 | CD 108 AAT>GAT [Asn>Asp] | Hb A2-Meizhou | HBD:c.325A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64533 |
1402 | (Hb Anti-Lepore P-Congo) | Hb P-Congo | NG_000007.3:g.64557_71923dup | δ, β | Causative | δ-chain variant | NG_000007.3 | 64557 |
1385 | CD 116 CGC>CAC [Arg>His] | Hb A2-Coburg | HBD:c.350G>A | δ | Causative | δ-chain variant | NG_000007.3 | 64558 |
3314 | CD 116 CGC>CCC [Arg>Pro] | Hb A2-Bornova | HBD:c.350G>C | δ | Causative | δ-chain variant | NG_000007.3 | 64558 |
3318 | CD 116 CGC>CTC [Arg>Leu] (Hb A2-India) | Hb A2-Lepore | HBD:c.350G>T | δ | Causative | δ-chain variant | NG_000007.3 | 64558 |
1386 | CD 117 AAC>GAC | Hb A2-Liangcheng | HBD:c.352A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64560 |
2363 | CD 119 GGC>GAC [Gly>Asp] | Hb A2-Lewisburg | HBD:c.359G>A | δ | Causative | δ-chain variant | NG_000007.3 | 64567 |
3843 | CD 120 AAG>ACG [Lys>Thr] | Hb A2-Liangqing | HBD:c.362A>C | δ | Causative | δ-chain variant | NG_000007.3 | 64570 |
3058 | CD 121 GAA>AAA [Glu>Lys] | Hb A2-Fengshun | HBD:c.364G>A | δ | Causative | δ-chain variant | NG_000007.3 | 64572 |
1387 | CD 121 GAA>GTA | Hb A2-Manzanares | HBD:c.365A>T | δ | Causative | δ-chain variant | NG_000007.3 | 64573 |
4012 | CD 123 ACC>GCC [Thr>Ala] | Hb A2-Kuching | HBD:c.370A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64578 |
1388 | CD 125 CAA>GAA | Hb A2-Zagreb | HBD:c.376C>G | δ | Causative | δ-chain variant | NG_000007.3 | 64584 |
4034 | CD 125 CAA>CGA [Gln>Arg] | Hb A2-Tongchuan | HBD:c.377A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64585 |
3546 | CD 130 TAT>-AT | Hb A2-Gaslini 1 | HBD:c.391delT | δ | Causative | δ-chain variant | NG_000007.3 | 64599 |
3490 | CD 131 CAG>GAG [Gln>Glu] | Hb A2-Puer | HBD:c.394C>G | δ | Causative | δ-chain variant | NG_000007.3 | 64602 |
1389 | CD 133 GTG>GCG | Hb A2-Ninive | HBD:c.401T>C | δ | Causative | δ-chain variant | NG_000007.3 | 64609 |
1390 | CD 136 GGT>GAT [Gly>Asp] | Hb A2-Babinga | HBD:c.410G>A | δ | Causative | δ-chain variant | NG_000007.3 | 64618 |
2482 | CD 137 -GTG [-Val] (Hb Anti-Lepore Lincoln Park) | Hb Lincoln Park | HBD:c.412_414delGTG | δ | Causative | δ-chain variant, Haemolytic anaemia | NG_000007.3 | 64620 |
1391 | CD 140 GCC>GTC | Hb A2-Bagheria | HBD:c.422C>T | δ | Causative | δ-chain variant | NG_000007.3 | 64630 |
2524 | CD 142 GCT>CCT [Ala>Pro] | N/A | HBD:c.427C>A | δ | Causative | δ-chain variant | NG_000007.3 | 64635 |
1393 | CD 142 GCT>GAT [Ala>Asp] | Hb A2-Fitzroy | HBD:c.428C>A | δ | Causative | δ-chain variant | NG_000007.3 | 64636 |
2392 | CD 143 CAC>TAC [His>Tyr] | Hb Noah Mehmet Oeztuerk | HBD:c.430C>T | δ | Causative | δ-chain variant | NG_000007.3 | 64638 |
2421 | CD 143 CAC>GAC [His>Asp] | Hb A2-Leuven | HBD:c.430C>G | δ | Causative | δ-chain variant | NG_000007.3 | 64638 |
2989 | CD 143 CAC>CGC [His>Arg] (Hb A2-Abruzzo) | Hb A2-Leuven II | HBD:c.431A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64639 |
3376 | CD 144 AAG>GAG [Lys>Glu] | Hb A2-Angola | HBD:c.433A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64641 |
2349 | CD 144 AAG>ACG [Lys>Thr] | Hb A2-San Floro | HBD:c.434A>C | δ | Causative | δ-chain variant | NG_000007.3 | 64642 |
1394 | CD 146 CAT>CGT | Hb A2-Monreale | HBD:c.440A>G | δ | Causative | δ-chain variant | NG_000007.3 | 64648 |
790 | CD 1 GTG>ATG | Hb South Florida | HBB:c.4G>A | β | Causative | β-chain variant | NG_000007.3 | 70598 |
791 | CD 1 GTG>TTG | Hb Niigata | HBB:c.4G>T | β | Causative | β-chain variant | NG_000007.3 | 70598 |
792 | CD 1 GTG>GGG | Hb Watford | HBB:c.5T>G | β | Causative | β-chain variant | NG_000007.3 | 70599 |
793 | CD 1 GTG>GCG | Hb Raleigh | HBB:c.5T>C | β | Causative | β-chain variant | NG_000007.3 | 70599 |
794 | CD 1 GTG>GAG | Hb Doha | HBB:c.5T>A | β | Causative | β-chain variant | NG_000007.3 | 70599 |
795 | CD 2 CAT>TAT | Hb Fukuoka | HBB:c.7C>T | β | Causative | β-chain variant | NG_000007.3 | 70601 |
2542 | CD 2 CAT>AAT [His>Asn] | Hb Franklin Park | HBB:c.7C>A | β | Causative | β-chain variant | NG_000007.3 | 70601 |
796 | CD 2 CAT>CCT [His>Pro] (Hb Long Island-Marseille, Hb Agrigente) | Hb Marseille | HBB:c.8A>C | β | Causative | β-chain variant | NG_000007.3 | 70602 |
797 | CD 2 CAT>CTT | Hb Graz | HBB:c.8A>T | β | Causative | β-chain variant | NG_000007.3 | 70602 |
799 | CD 2 CAT>CGT | Hb Deer Lodge | HBB:c.8A>G | β | Causative | β-chain variant | NG_000007.3 | 70602 |
800 | CD 2 CAT>CAA or CAG | Hb Okayama | HBB:c.9T>A | HBB:c.9T>G | β | Causative | β-chain variant | NG_000007.3 | 70603 |
802 | CD 3 CTG>GTG [Leu>Val] | Hb Kamakura | HBB:c.10C>G | β | Causative | β-chain variant | NG_000007.3 | 70604 |
2327 | CD 3 CTG>ATG [Leu>Met] | Hb Niguarda | HBB:c.10C>A | β | Causative | β-chain variant | NG_000007.3 | 70604 |
3794 | CD 3 (CTG>AAG) [Leu>Lys] | Hb Jiangnan | HBB:c.10_11delinsAA | β | Causative | β-chain variant | NG_000007.3 | 70604 |
803 | CD 3 CTG>CAG [Leu>Gln] | Hb Santo Domingo | HBB:c.11T>A | β | Causative | β-chain variant | NG_000007.3 | 70605 |
2359 | CD 3 CTG>CCG [Leu>Pro] | Hb Jabalpur | HBB:c.11T>C | β | Causative | β-chain variant | NG_000007.3 | 70605 |
3878 | CD 3 CTG>CGG [Leu>Arg] | Hb Sedgwick | HBB:c.11T>G | β | Causative | β-chain variant | NG_000007.3 | 70605 |
2326 | CD 4 ACT>CCT [Thr>Pro] | Hb Benin City | HBB:c.13A>C | β | Causative | β-chain variant | NG_000007.3 | 70607 |
804 | CD 4 ACT>AAT | Hb Wurzburg | HBB:c.14C>A | β | Causative | β-chain variant | NG_000007.3 | 70608 |
3949 | CD 4 ACT>ATT [Thr>Ile] | Hb Fox Point | HBB:c.14C>T | β | Causative | β-chain variant | NG_000007.3 | 70608 |
805 | CD 5 CCT>TCT | Hb Tyne | HBB:c.16C>T | β | Causative | β-chain variant | NG_000007.3 | 70610 |
806 | CD 5 CCT>GCT [Pro>Ala] (Hb Hinchingbrooke) | Hb Gorwihl | HBB:c.16C>G | β | Causative | β-chain variant | NG_000007.3 | 70610 |
807 | CD 5 CCT>CGT | Hb Warwickshire | HBB:c.17C>G | β | Causative | β-chain variant | NG_000007.3 | 70611 |
2321 | CD 5 CCT>CTT [Pro>Leu] | Hb Aix-les-Bains | HBB:c.17C>T | β | Causative | β-chain variant | NG_000007.3 | 70611 |
808 | CD 6 GAG>AAG; CD 95 AAG>GAG | Hb Arlington Park | HBB:c.[19G>A;286A>G] | β | Causative | β-chain variant | NG_000007.3 | 70613 |
809 | CD 6 GAG>AAG [Glu>Lys] and CD 98 GTG>ATG [Val>Met] | Hb Kingsbury | HBB:c.[19G>A ;295G>A] | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70613 |
810 | CD 6 GAG>AAG [Glu>Lys] | HbC | HBB:c.19G>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70613 |
811 | CD 6 GAG>AAG [Glu>Lys]; CD 37 TGG>AGG or CGG [Trp>Arg] | Hb C-Rothschild | HBB:c.[19G>A;112T>A] | HBB:c.[19G>A;112T>C] | β | Causative | β-chain variant | NG_000007.3 | 70613, 70836 |
812 | CD 6 GAG>AAG; CD 83 GGC>GAC | Hb C-New Cross | HBB:c.[19G>A;251G>A] | β | Causative | β-chain variant | NG_000007.3 | 70613 |
813 | CD 6 GAG>CAG | Hb Machida | HBB:c.19G>C | β | Causative | β-chain variant | NG_000007.3 | 70613 |
814 | CD 6 GAG>GTG | Hb S-South End | HBB:c.[20A>T;399A>C] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
815 | CD 6 GAG>GTG; CD 23 GTT>ATT | Hb S-Antilles | HBB:c.[20A>T;70G>A] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
816 | CD 6 GAG>GTG; CD 58 CCT>CGT | Hb C-Ziguinchor | HBB:c.[20A>T;176C>G] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
817 | CD 6 GAG>GTG; CD 73 GAT>AAT | Hb C-Harlem | HBB:c.[20A>T;220G>A] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
818 | CD 6 GAG>GTG; CD 82AAG>AAT or AAC | Hb S-Providence | HBB:c.[20A>T;249G>C] | HBB:c.[20A>T;249G>T] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
819 | CD 6 GAG>GTG; CD 142 GCC>GTC | Hb S-Travis | HBB:c.[20A>T;428C>T] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
820 | CD 6 GAG>GTG [Glu>Val]; CD 37 TGG>GGG [Trp>Gly] | Hb C-Ndjamena; Hb S-Northwick | HBB:c.[20A>T;112T>G] | β | Causative | β-chain variant | NG_000007.3 | 70614, 70836 |
821 | CD 6 GAG>GTG; CD 121 GAA>AAA | Hb S-Oman | HBB:c.[20A>T;364G>A] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
822 | CD 6 GAG>GTG [Glu>Val], CD 8 AAG>ACG [Lys>Thr] | Hb S-Clichy | HBB:c.[20A>T;26A>C] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
823 | CD 6 GAG>GTG; CD 90 GAG>AAG | Hb S-Cameroon | HBB:c.[20A>T;271G>A] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
824 | CD 6 GAG>GTG [Glu>Val] (Sickle-cell) | HbS | HBB:c.20A>T | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70614 |
825 | CD 6 GAG>GTG; CD 68 CTC>TTC | Hb Jamaica Plain | HBB:c.[20A>T;205C>T] | β | Causative | β-chain variant | NG_000007.3 | 70614 |
826 | CD 6 GAG>GCG | Hb G-Makassar | HBB:c.20A>C | β | Causative | β-chain variant | NG_000007.3 | 70614 |
827 | CD 6 GAG>GGG [Glu>Gly] | Hb Lavagna | HBB:c.20A>G | β | Causative | β-chain variant | NG_000007.3 | 70614 |
2440 | CD 6 GAG>GTG [Glu>Val] AND CD 65 AAG>GAG [Lys>Glu] | Hb S-Sao Paulo | HBB:c.[20A>T ;196A>G] | β | Causative | β-chain variant | NG_000007.3 | 70614, 70920 |
3324 | CD 6 GAG>GTG [Glu>Val]; CD 139 AAT>AGT [Asn>Ser] | Hb S-Wake | HBB:c.[20A>T;419A>G] | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70614, 71993 |
828 | CD 7 (-GAG) [-Glu] (Hb Xinyi) | Hb Leiden | HBB:c.22_24delGAG | β | Causative | β-chain variant | NG_000007.3 | 70616 |
829 | CD 7 GAG>AAG | Hb G-Siriraj | HBB:c.22G>A | β | Causative | β-chain variant | NG_000007.3 | 70616 |
2400 | CD 7 GAG>CAG [Glu>Gln] (Hb Bellevue III) | Hb Vellore | HBB:c.22G>C | β | Causative | β-chain variant | NG_000007.3 | 70616 |
830 | CD 7 GAG>GGG | Hb G-San José | HBB:c.23A>G | β | Causative | β-chain variant | NG_000007.3 | 70617 |
2963 | CD 7 GAG>GTG [Glu>Val] | Hb Haaglanden | HBB:c.23A>T | β | Causative | β-chain variant | NG_000007.3 | 70617 |
2382 | CD 7 GAG>GAT [Glu>Asp] | Hb Stockholm | HBB:c.24G>T | β | Causative | β-chain variant | NG_000007.3 | 70618 |
831 | CD 8 AAG>CAG [Lys>Gln] | Hb J-Luhe | HBB:c.25A>C | β | Causative | β-chain variant | NG_000007.3 | 70619 |
832 | CD 8 AAG>GAG | Hb N-Timone | HBB:c.25A>G | β | Causative | β-chain variant | NG_000007.3 | 70619 |
833 | CD 8 AAG>ACG | Hb Rio Grande | HBB:c.26A>C | β | Causative | β-chain variant | NG_000007.3 | 70620 |
834 | CD 8 AAG>ATG | Hb Nakano | HBB:c.26A>T | β | Causative | β-chain variant | NG_000007.3 | 70620 |
835 | CD 8 AAG>AGG [Lys>Arg] | Hb Lucknow | HBB:c.26A>G | β | Causative | β-chain variant | NG_000007.3 | 70620 |
836 | CD 8 AAG>AAC | Hb Limassol | HBB:c.27G>C | β | Causative | β-chain variant | NG_000007.3 | 70621 |
837 | CD 9 TCT>TAT | Hb Brem-sur-Mer | HBB:c.29C>A | β | Causative | β-chain variant | NG_000007.3 | 70623 |
838 | CD 9 TCT>TGT | Hb Pôrto Alegre | HBB:c.29C>G | β | Causative | β-chain variant | NG_000007.3 | 70623 |
839 | CD 9 TCT>TAT; CD 121 GAA>CAA | Hb D-Agri | HBB:c.[29C>A;364G>C] | β | Causative | β-chain variant | NG_000007.3 | 70623 |
3401 | CD 9 TCT>TTT [Ser>Phe] | Hb Hengyang | HBB:c.29C>T | β | Causative | β-chain variant | NG_000007.3 | 70623 |
3399 | CD 9 TCT>TC- | Hb Antep | HBB:c.30delT | β | Causative | β-chain variant | NG_000007.3 | 70624 |
840 | CD 10 GCC>ACC [Ala>Thr] | Hb Belleville | HBB:c.31G>A | β | Causative | β-chain variant | NG_000007.3 | 70625 |
841 | CD 10 GCC>GTC | Hb Iraq-Halabja | HBB:c.32C>T | β | Causative | β-chain variant | NG_000007.3 | 70626 |
842 | CD 10 GCC>GAC | Hb Ankara | HBB:c.32C>A | β | Causative | β-chain variant | NG_000007.3 | 70626 |
843 | CD 11 GTT>ATT | Hb Hamilton | HBB:c.34G>A | β | Causative | β-chain variant | NG_000007.3 | 70628 |
844 | CD 11 GTT>TTT | Hb Washtenaw | HBB:c.34G>T | β | Causative | β-chain variant | NG_000007.3 | 70628 |
845 | CD 11 GTT>ATT; CD 121 GAA>AAA | Hb O-Tibesti | HBB:c.[34G>A;364G>A] | β | Causative | β-chain variant | NG_000007.3 | 70628 |
3297 | CD 11-13 (-9bp): (-GTTACTGCC) | Hb JC-Paz | HBB:c.34_42delGTTACTGCC | β | Causative | β-chain variant | NG_000007.3 | 70628 |
847 | CD 11 GTT>GAT | Hb Windsor | HBB:c.35T>A | β | Causative | β-chain variant | NG_000007.3 | 70629 |
2492 | CD 12 ACT>CCT [Thr>Pro] (Hb Feilding) | Hb Ashburton | HBB:c.37A>C | β | Causative | β-chain variant | NG_000007.3 | 70631 |
2543 | CD 12 ACT>ATT [Thr>Ile] | Hb William-Harvey | HBB:c.38C>T | β | Causative | β-chain variant | NG_000007.3 | 70632 |
3359 | CD 13 GCC>ACC [Ala>Thr] (Hb Chuxiong) | Hb Tower Hamlets | HBB:c.40G>A | β | Causative | β-chain variant | NG_000007.3 | 70634 |
848 | CD 13 GCC>GAC | Hb J-Lens | HBB:c.41C>A | β | Causative | β-chain variant | NG_000007.3 | 70635 |
3248 | CD 13 GCC>GTC [Ala>Val] | Hb Yulin | HBB:c.41C>T | β | Causative | β-chain variant | NG_000007.3 | 70635 |
849 | CD 14 CTG>CCG | Hb Saki | HBB:c.44T>C | β | Causative | β-chain variant | NG_000007.3 | 70638 |
850 | CD 14 CTG>CGG | Hb Sogn | HBB:c.44T>G | β | Causative | β-chain variant | NG_000007.3 | 70638 |
851 | CD 15 TGG>GGG | Hb Randwick | HBB:c.46T>G | β | Causative | β-chain variant | NG_000007.3 | 70640 |
852 | CD 15 TGG>AGG or CGG | Hb Belfast | HBB:c.46T>A | HBB:c.46T>C | β | Causative | β-chain variant | NG_000007.3 | 70640 |
2464 | CD 15 TGG>TGC or TGT [Trp>Cys] | Hb Garston | HBB:c.48G>Y | β | Causative | β-chain variant | NG_000007.3 | 70642 |
853 | CD 16 GGC>CGC | Hb D-Bushman | HBB:c.49G>C | β | Causative | β-chain variant | NG_000007.3 | 70643 |
2374 | CD 16 GGC>TGC [Gly>Cys] | Hb Whitmire | HBB:c.49G>T | β | Causative | β-chain variant | NG_000007.3 | 70643 |
854 | CD 16 GGC>GAC (Hb J-Georgia , Hb J-Ireland , Hb J-Trinidad , Hb N-New Haven) | Hb J-Baltimore | HBB:c.50G>A | β | Causative | β-chain variant | NG_000007.3 | 70644 |
856 | CD 17 AAG>GAG | Hb Nagasaki | HBB:c.52A>G | β | Causative | β-chain variant | NG_000007.3 | 70646 |
857 | CD 17 AAG>CAG (Hb Nicosia) | Hb Nikosia | HBB:c.52A>C | β | Causative | β-chain variant | NG_000007.3 | 70646 |
855 | CD 17-19 (-GGTGAA) | Hb Lyon | HBB:c.54_59del | β | Causative | β-chain variant | NG_000007.3 | 70648 |
858 | CD 17 AAG>AAC or AAT | Hb J-Amiens | HBB:c.54G>C | HBB:c.54G>T | β | Causative | β-chain variant | NG_000007.3 | 70648 |
859 | CD 18 GTG>ATG | Hb Baden | HBB:c.55G>A | β | Causative | β-chain variant | NG_000007.3 | 70649 |
3005 | CD 18 GTG>CTG [Val>Leu] | Hb Bhubaneswar | HBB:c.55G>C | β | Causative | β-chain variant | NG_000007.3 | 70649 |
860 | CD 18 GTG>GGG | Hb Sinai-Baltimore | HBB:c.56T>G | β | Causative | β-chain variant | NG_000007.3 | 70650 |
861 | CD 19 AAC>GAC | Hb Alamo | HBB:c.58A>G | β | Causative | β-chain variant | NG_000007.3 | 70652 |
863 | CD 19 AAC>AAA or AAG | Hb D-Ouled Rabah | HBB:c.60C>A | HBB:c.60C>G | β | Causative | β-chain variant | NG_000007.3 | 70654 |
864 | CD 20 GTG>ATG | Hb Olympia | HBB:c.61G>A | β | Causative | β-chain variant | NG_000007.3 | 70655 |
865 | CD 20 GTG>GGG | Hb Uxbridge | HBB:c.62T>G | β | Causative | β-chain variant | NG_000007.3 | 70656 |
866 | CD 20 GTG>GAG | Hb Trollhättan | HBB:c.62T>A | β | Causative | β-chain variant | NG_000007.3 | 70656 |
2974 | CD 20 GTG>GCG [Val>Ala] | Hb Howden | HBB:c.62T>C | β | Causative | β-chain variant | NG_000007.3 | 70656 |
867 | CD 21 GAT>TAT | Hb Yusa | HBB:c.64G>T | β | Causative | β-chain variant | NG_000007.3 | 70658 |
868 | CD 21 GAT>CAT | Hb Karlskoga | HBB:c.64G>C | β | Causative | β-chain variant | NG_000007.3 | 70658 |
869 | CD 21 GAT>AAT | Hb Cocody | HBB:c.64G>A | β | Causative | β-chain variant | NG_000007.3 | 70658 |
870 | CD 21 GAT>GGT | Hb Connecticut | HBB:c.65A>G | β | Causative | β-chain variant | NG_000007.3 | 70659 |
871 | CD 21 GAT>GTT | Hb Rocky Mountain | HBB:c.65A>T | β | Causative | β-chain variant | NG_000007.3 | 70659 |
873 | CD 22 GAA>CAA | Hb D-Iran | HBB:c.67G>C | β | Causative | β-chain variant | NG_000007.3 | 70661 |
874 | CD 22 GAA>AAA | Hb E-Saskatoon | HBB:c.67G>A | β | Causative | β-chain variant | NG_000007.3 | 70661 |
875 | CD 22 GAA>GTA | Hb D-Granada | HBB:c.68A>T | β | Causative | β-chain variant | NG_000007.3 | 70662 |
876 | CD 22 GAA>GCA (Hb G-Hsin Chu, Hb G-Saskatoon, Hb G-Taegu) | Hb G-Coushatta | HBB:c.68A>C | β | Causative | β-chain variant | NG_000007.3 | 70662 |
877 | CD 22 GAA>GGA | Hb G-Taipei | HBB:c.68A>G | β | Causative | β-chain variant | NG_000007.3 | 70662 |
872 | CD 22-26 (-12bp) | Hb Olinda | HBB:c.69_80delAGTTGGTGGTGA | β | Causative | β-chain variant | NG_000007.3 | 70663 |
2330 | CD 22 GAA>GAT [Glu>Asp] | Hb Bury | HBB:c.69A>T | β | Causative | β-chain variant | NG_000007.3 | 70663 |
879 | CD 23 GTT>ATT [Val>Ile] | Hb Saveh | HBB:c.70G>A | β | Causative | β-chain variant | NG_000007.3 | 70664 |
880 | CD 23 GTT>TTT | Hb Palmerston North | HBB:c.70G>T | β | Causative | β-chain variant | NG_000007.3 | 70664 |
878 | CD 23/24 (GTTGGT>GGT) | Hb Freiburg | HBB:c.71_73del | β | Causative | β-chain variant | NG_000007.3 | 70665 |
881 | CD 23 GTT>GCT | Hb Zoeterwoude | HBB:c.71T>C | β | Causative | β-chain variant | NG_000007.3 | 70665 |
882 | CD 23 GTT>GGT | Hb Miyashiro | HBB:c.71T>G | β | Causative | β-chain variant | NG_000007.3 | 70665 |
883 | CD 23 GTT>GAT | Hb Strasbourg | HBB:c.71T>A | β | Causative | β-chain variant | NG_000007.3 | 70665 |
885 | CD 24 GGT>CGT | Hb Riverdale-Bronx | HBB:c.73G>C | β | Causative | β-chain variant | NG_000007.3 | 70667 |
886 | CD 24 GGT>GAT [Gly>Asp] | Hb Moscva | HBB:c.74G>A | β | Causative | β-chain variant | NG_000007.3 | 70668 |
887 | CD 24 GGT>GTT | Hb Savannah | HBB:c.74G>T | β | Causative | β-chain variant | NG_000007.3 | 70668 |
888 | CD 25 GGT>CGT | Hb G-Taiwan-Ami | HBB:c.76G>C | β | Causative | β-chain variant | NG_000007.3 | 70670 |
2452 | CD 25 GGT>AGT [Gly>Ser] | Hb Brazzaville | HBB:c.76G>A | β | Causative | β-chain variant | NG_000007.3 | 70670 |
889 | CD 25 GGT>GAT | Hb J-Auckland | HBB:c.77G>A | β | Causative | β-chain variant | NG_000007.3 | 70671 |
3306 | CD 25/26 -GTG [-Gly] (Hb Higashitochigi, Hb HT) | Hb M Dothan | HBB:c.77_79delGTG | β | Causative | β-chain variant | NG_000007.3 | 70671 |
891 | CD 26 GAG>AAG, CD 104 AGG>ACG | Hb Corbeil | HBB:c.[79G>A;314G>C] | β | Causative | β-chain variant | NG_000007.3 | 70673 |
892 | CD 26 GAG>AAG; CD 121 GAA>CAA | Hb T-Cambodia | HBB:c.[79G>A;364G>C] | β | Causative | β-chain variant | NG_000007.3 | 70673 |
3035 | CD 26 GAG>CAG [Glu>Gln] | Hb King's Mill | HBB:c.79G>C | β | Causative | β-chain variant | NG_000007.3 | 70673 |
893 | CD 26 GAG>GGG | Hb Aubenas | HBB:c.80A>G | β | Causative | β-chain variant | NG_000007.3 | 70674 |
894 | CD 26 GAG>GCG | Hb Tripoli | HBB:c.80A>C | β | Causative | β-chain variant | NG_000007.3 | 70674 |
895 | CD 26 GAG>GTG [Glu>Val] | Hb Henri Mondor | HBB:c.80A>T | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70674 |
2403 | CD 26 GAG>GAC or GAT [Glu>Asp] | Hb Marijampolė | HBB:c.81G>Y | β | Causative | β-chain variant | NG_000007.3 | 70675 |
897 | CD 27 GCC>GTC | Hb Grange-Blanche | HBB:c.83C>T | β | Causative | β-chain variant | NG_000007.3 | 70677 |
898 | CD 27 GCC>GAC | Hb Volga | HBB:c.83C>A | β | Causative | β-chain variant | NG_000007.3 | 70677 |
899 | CD 27 GCC>GGC [Ala>Gly] | Hb Siirt | HBB:c.83C>G | β | Causative | β-chain variant | NG_000007.3 | 70677 |
900 | CD 28 CTG>ATG [Leu>Met] | Hb Chile | HBB:c.85C>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70679 |
901 | CD 28 CTG>CCG [Leu>Pro] | Hb Genova | HBB:c.86T>C | β | Causative | β-chain variant | NG_000007.3 | 70680 |
902 | CD 28 CTG>CAG [Leu>Gln] | Hb Saint Louis | HBB:c.86T>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70680 |
904 | CD 29 GGC>AGC [Gly>Ser] | Hb Tizi-Ouzou | HBB:c.88G>A | β | Causative | β-chain variant | NG_000007.3 | 70682 |
2523 | CD 29 GGC>CGC [Gly>Arg] | Hb Dompierre | HBB:c.88G>C | β | Causative | β-chain variant | NG_000007.3 | 70682 |
905 | CD 29 GGC>GAC | Hb Lufkin | HBB:c.89G>A | β | Causative | β-chain variant | NG_000007.3 | 70683 |
907 | CD 30 AGG>AGT [Arg>Ser] | Hb Tacoma | HBB:c.93G>T | β | Causative | β-chain variant | NG_000007.3 | 70817 |
908 | CD 31 CTG>GTG | Hb Badalona | HBB:c.94C>G | β | Causative | β-chain variant | NG_000007.3 | 70818 |
909 | CD 31 CTG>CGG | Hb Hakkari | HBB:c.95T>G | β | Causative | β-chain variant | NG_000007.3 | 70819 |
910 | CD 31 CTG>CCG | Hb Yokohama | HBB:c.95T>C | β | Causative | β-chain variant | NG_000007.3 | 70819 |
911 | CD 32 CTG>GTG | Hb Muscat | HBB:c.97C>G | β | Causative | β-chain variant | NG_000007.3 | 70821 |
912 | CD 32 CTG>CCG | Hb Perth | HBB:c.98T>C | β | Causative | β-chain variant | NG_000007.3 | 70822 |
913 | CD 32 CTG>CAG [Leu>Gln] | Hb Clermont Ferrand | HBB:c.98T>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70822 |
915 | CD 32 CTG>CGG [Leu>Arg] | Hb Castilla | HBB:c.98T>G | β | Causative | β-chain variant | NG_000007.3 | 70822 |
916 | CD 33 GTG>ATG | Hb Rio Claro | HBB:c.100G>A | β | Causative | β-chain variant | NG_000007.3 | 70824 |
3364 | CD 33 GTG>TTG [Val>Leu] | Hb Venissieux | HBB:c.100G>T | β | Causative | β-chain variant | NG_000007.3 | 70824 |
919 | CD 34 GTC>CTC | Hb Nantes | HBB:c.103G>C | β | Causative | β-chain variant | NG_000007.3 | 70827 |
920 | CD 34 GTC>TTC | Hb Pitie-Salpetriere | HBB:c.103G>T | β | Causative | β-chain variant | NG_000007.3 | 70827 |
921 | CD 34 GTC>GAC | Hb Santander | HBB:c.104T>A | β | Causative | β-chain variant | NG_000007.3 | 70828 |
2331 | CD 35 TAC>CAC [Tyr>His] | Hb Fulwood | HBB:c.106T>C | β | Causative | β-chain variant | NG_000007.3 | 70830 |
3795 | CD 35 TAC>GAC [Tyr>Asp] | Hb Oristano | HBB:c.106T>G | β | Causative | β-chain variant | NG_000007.3 | 70830 |
922 | CD 35 TAC>TTC [Tyr>Phe] | Hb Philly | HBB:c.107A>T | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70831 |
923 | CD 36 CCT>ACT | Hb Linköping | HBB:c.109C>A | β | Causative | β-chain variant | NG_000007.3 | 70833 |
924 | CD 36 CCT>GCT | Hb Brie Comte Robert | HBB:c.109C>G | β | Causative | β-chain variant | NG_000007.3 | 70833 |
925 | CD 36 CCT>TCT | Hb North Chicago | HBB:c.109C>T | β | Causative | β-chain variant | NG_000007.3 | 70833 |
926 | CD 36 CCT>CGT [Pro>Arg] | Hb Sunnybrook | HBB:c.110C>G | β | Causative | β-chain variant | NG_000007.3 | 70834 |
927 | CD 36 CCT>CAT | Hb Vila Real | HBB:c.110C>A | β | Causative | β-chain variant | NG_000007.3 | 70834 |
928 | CD 37 TGG>AGG [Trp>Arg] | Hb Rothschild | HBB:c.112T>A | β | Causative | β-chain variant | NG_000007.3 | 70836 |
929 | CD 37 TGG>GGG | Hb Howick | HBB:c.112T>G | β | Causative | β-chain variant | NG_000007.3 | 70836 |
930 | CD 37 TGG>TCG | Hb Hirose | HBB:c.113G>C | β | Causative | β-chain variant | NG_000007.3 | 70837 |
3918 | CD 37 TGG>TTG [Trp>Leu] | Hb Alessandria | HBB:c.113G>T | β | Causative | β-chain variant | NG_000007.3 | 70837 |
931 | CD 37 TGG>TGT [Trp>Cys] (Hb Greendale) | Hb Kent | HBB:c.114G>T | β | Causative | β-chain variant | NG_000007.3 | 70838 |
3282 | CD 37 TGG>TGC [Trp>Cys] (Hb Kent) | N/A | HBB:c.114G>C | β | Causative | β-chain variant | NG_000007.3 | 70838 |
932 | CD 38 ACC>CCC | Hb Hazebrouck | HBB:c.115A>C | β | Causative | β-chain variant | NG_000007.3 | 70839 |
4112 | CD 38 ACC>GCC [Thr>Ala] | Hb Oviedo | HBB:c.115A>G | β | Causative | β-chain variant | NG_000007.3 | 70839 |
933 | CD 38 ACC>AAC | Hb Hinwil | HBB:c.116C>A | β | Causative | β-chain variant | NG_000007.3 | 70840 |
934 | CD 38 ACC>ATC | Hb La Coruna | HBB:c.116C>T | β | Causative | β-chain variant | NG_000007.3 | 70840 |
2280 | CD 38 ACC>AGC | N/A | HBB:c.116C>G | β | Causative | β-chain variant | NG_000007.3 | 70840 |
935 | CD 39 CAG>AAG | Hb Alabama | HBB:c.118C>A | β | Causative | β-chain variant | NG_000007.3 | 70842 |
936 | CD 39 CAG>GAG | Hb Vaasa | HBB:c.118C>G | β | Causative | β-chain variant | NG_000007.3 | 70842 |
937 | CD 39 CAG>CGG [Gln>Arg] | Hb Tianshui | HBB:c.119A>G | β | Causative | β-chain variant | NG_000007.3 | 70843 |
2962 | CD 39 CAG>CCG [Gln>Pro] | Hb Hyden | HBB:c.119A>C | β | Causative | β-chain variant | NG_000007.3 | 70843 |
938 | CD 39 CAG>CAC | Hb San Bruno | HBB:c.120G>C | β | Causative | β-chain variant | NG_000007.3 | 70844 |
4045 | CD 40 AGG>GGG [Arg>Gly] | Hb Montpellier | HBB:c.121A>G | β | Causative | β-chain variant | NG_000007.3 | 70845 |
939 | CD 40 AGG>AAG [Arg>Lys] | Hb Athens-GA | HBB:c.122G>A | β | Causative | β-chain variant | NG_000007.3 | 70846 |
940 | CD 40 AGG>ATG [Arg>Met] | Hb Taipei-Tien | HBB:c.122G>T | β | Causative | β-chain variant | NG_000007.3 | 70846 |
2544 | CD 40 AGG>ACG [Arg>Thr] | Hb Alcorn County | HBB:c.122G>C | β | Causative | β-chain variant | NG_000007.3 | 70846 |
941 | CD 40 AGG>AGT [Arg>Ser] | Hb Austin | HBB:c.123G>T | β | Causative | β-chain variant | NG_000007.3 | 70847 |
3004 | CD 41 TTC>GTC [Phe>Val] | Hb Valme | HBB:c.124T>G | β | Causative | β-chain variant | NG_000007.3 | 70848 |
942 | CD 41 TTC>TGC | Hb Ilmenau | HBB:c.125T>G | β | Causative | β-chain variant | NG_000007.3 | 70849 |
943 | CD 41 TTC>TCC | Hb Denver | HBB:c.125T>C | β | Causative | β-chain variant | NG_000007.3 | 70849 |
944 | CD 41 TTC>TAC | Hb Mequon | HBB:c.125T>A | β | Causative | β-chain variant | NG_000007.3 | 70849 |
2387 | CD 67 GTG>ATG [Val>Met] AND CD 41 TTC>TTG [Phe>Leu] | Hb Brevedent | HBB:c.[202G>A ;126C>G] | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70850 |
2972 | CD 41 TTC>TTA [Phe>Leu] | Hb Wilton | HBB:c.126C>A | β | Causative | β-chain variant | NG_000007.3 | 70850 |
945 | CD 42 (-TTT) | Hb Bruxelles | HBB:c.127_129delTTT | β | Causative | β-chain variant | NG_000007.3 | 70851 |
947 | CD 42 TTT>CTT [Phe>Leu] | Hb Louisville | HBB:c.127T>C | β | Causative | β-chain variant | NG_000007.3 | 70851 |
948 | CD 42 TTT>GTT (Hb Warsaw) | Hb Sendagi | HBB:c.127T>G | β | Causative | β-chain variant | NG_000007.3 | 70851 |
2461 | CD 42 TTT>ATT [Phe>Ile] | Hb Oslo | HBB:c.127T>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70851 |
949 | CD 42 TTT>TCT [Phe>Ser] | Hb Hammersmith | HBB:c.128T>C | β | Causative | β-chain variant | NG_000007.3 | 70852 |
2332 | CD 42 TTT>TGT [Phe>Cys] | Hb Little Venice | HBB:c.128T>G | β | Causative | β-chain variant | NG_000007.3 | 70852 |
4079 | CD 42 TTT>TTA [Phe>Leu] | Hb Suqian | HBB:c.129T>A | β | Causative | β-chain variant | NG_000007.3 | 70853 |
950 | CD 43 GAG>CAG | Hb Hoshida | HBB:c.130G>C | β | Causative | β-chain variant | NG_000007.3 | 70854 |
951 | CD 43 GAG>AAG [Glu>Lys] | Hb Hornchurch | HBB:c.130G>A | β | Causative | β-chain variant | NG_000007.3 | 70854 |
946 | CD 43-46 (-9bp) | Hb Niteroi | HBB:c.131_139del | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70855 |
952 | CD 43 GAG>GGG [Glu>Gly] | Hb Haringey | HBB:c.131A>G | β | Causative | β-chain variant | NG_000007.3 | 70855 |
953 | CD 43 GAG>GCG | Hb G-Galveston | HBB:c.131A>C | β | Causative | β-chain variant | NG_000007.3 | 70855 |
954 | CD 44 TCC>TGC | Hb Mississippi | HBB:c.134C>G | β | Causative | β-chain variant | NG_000007.3 | 70858 |
3969 | CD 44 TCC>TTC [Ser>Phe] | Hb Narges Lab | HBB:c.134C>T | β | Causative | β-chain variant | NG_000007.3 | 70858 |
2531 | CD 45 TTT>GTT [Phe>Val] | Hb Duc Pho | HBB:c.136T>G | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70860 |
955 | CD 45 TTT>TCT | Hb Cheverly | HBB:c.137T>C | β | Causative | β-chain variant | NG_000007.3 | 70861 |
956 | CD 45 TTT>TAT [Phe>Tyr] | Hb Den Haag | HBB:c.137T>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70861 |
957 | CD 45 TTT>TGT | Hb Arta | HBB:c.137T>G | β | Causative | β-chain variant | NG_000007.3 | 70861 |
958 | CD 46 GGG>AGG | Hb Gainesville-GA | HBB:c.139G>A | β | Causative | β-chain variant | NG_000007.3 | 70863 |
3567 | CD 46 GGG>CGG [Gly>Arg] | Hb Cenxi | HBB:c.139G>C | β | Causative | β-chain variant | NG_000007.3 | 70863 |
959 | CD 46 GGG>GAG | Hb K-Ibadan | HBB:c.140G>A | β | Causative | β-chain variant | NG_000007.3 | 70864 |
960 | CD 47 GAT>AAT [Asp>Asn] | Hb G-Copenhagen | HBB:c.142G>A | β | Causative | β-chain variant | NG_000007.3 | 70866 |
961 | CD 47 GAT>CAT [Asp>His] | Hb Maryland | HBB:c.142G>C | β | Causative | β-chain variant | NG_000007.3 | 70866 |
962 | CD 47 GAT>TAT | Hb Maputo | HBB:c.142G>T | β | Causative | β-chain variant | NG_000007.3 | 70866 |
963 | CD 47 GAT>GCT | Hb Avicenna | HBB:c.143A>C | β | Causative | β-chain variant | NG_000007.3 | 70867 |
964 | CD 47 GAT>GGT | Hb Gavello | HBB:c.143A>G | β | Causative | β-chain variant | NG_000007.3 | 70867 |
965 | CD 47 GAT>GTT | Hb Muravera | HBB:c.143A>T | β | Causative | β-chain variant | NG_000007.3 | 70867 |
966 | CD 48 CTG>CGG | Hb Okaloosa | HBB:c.146T>G | β | Causative | β-chain variant | NG_000007.3 | 70870 |
967 | CD 48 CTG>CCG | Hb Bab-Saadoun | HBB:c.146T>C | β | Causative | β-chain variant | NG_000007.3 | 70870 |
3494 | CD 49 TCC>CCC [Ser>Pro] | Hb Yunnan | HBB:c.148T>C | β | Causative | β-chain variant | NG_000007.3 | 70872 |
968 | CD 49 TCC>TGC | Hb Colima | HBB:c.149C>G | β | Causative | β-chain variant | NG_000007.3 | 70873 |
969 | CD 49 TCC>TTC | Hb Las Palmas | HBB:c.149C>T | β | Causative | β-chain variant | NG_000007.3 | 70873 |
970 | CD 50 ACT>TCT [Thr>Ser] | Hb Zurich-Langstrasse | HBB:c.151A>T | β | Causative | β-chain variant | NG_000007.3 | 70875 |
971 | CD 50 ACT>AAG or AAA | Hb Edmonton | HBB:c.[152C>A;153T>A] | HBB:c.[152C>A;153T>G] | β | Causative | β-chain variant | NG_000007.3 | 70876 |
972 | CD 51 CCT>TCT, CD 52 GAT>AAT | Hb Grenoble | HBB:c.[154C>T;157G>A] | β | Causative | β-chain variant | NG_000007.3 | 70878 |
973 | CD 51 CCT>CAT | Hb North Manchester | HBB:c.155C>A | β | Causative | β-chain variant | NG_000007.3 | 70879 |
974 | CD 51 CCT>CGT | Hb Willamette | HBB:c.155C>G | β | Causative | β-chain variant | NG_000007.3 | 70879 |
975 | CD 52 GAT>TAT [Asp>Tyr] | Hb Languidic | HBB:c.157G>T | β | Causative | β-chain variant | NG_000007.3 | 70881 |
976 | CD 52 GAT>CAT | Hb Summer Hill | HBB:c.157G>C | β | Causative | β-chain variant | NG_000007.3 | 70881 |
977 | CD 52 GAT>AAT | Hb Osu Christiansborg | HBB:c.157G>A | β | Causative | β-chain variant | NG_000007.3 | 70881 |
978 | CD 52 GAT>GGT | Hb Hokusetsu | HBB:c.158A>G | β | Causative | β-chain variant | NG_000007.3 | 70882 |
979 | CD 52 GAT>GCT | Hb Ocho Rios | HBB:c.158A>C | β | Causative | β-chain variant | NG_000007.3 | 70882 |
980 | CD 52 GAT>GTT [Asp>Val] | Hb Akron | HBB:c.158A>T | β | Causative | β-chain variant | NG_000007.3 | 70882 |
982 | CD 53 GCT>ACT | Hb Acharnes | HBB:c.160G>A | β | Causative | β-chain variant | NG_000007.3 | 70884 |
2964 | CD 53 GCT>GTT [Ala>Val] | Hb Midnapore | HBB:c.161C>T | β | Causative | β-chain variant | NG_000007.3 | 70885 |
3368 | CD 54 GTT>CTT [Val>Leu] | Hb Askew | HBB:c.163G>C | β | Causative | β-chain variant | NG_000007.3 | 70887 |
983 | CD 54 GTT>GAT | Hb Jacksonville | HBB:c.164T>A | β | Causative | β-chain variant | NG_000007.3 | 70888 |
984 | CD 55 ATG>AAG | Hb Matera | HBB:c.167T>A | β | Causative | β-chain variant | NG_000007.3 | 70891 |
985 | CD 56 GGC>TGC | Hb Leeds | HBB:c.169G>T | β | Causative | β-chain variant | NG_000007.3 | 70893 |
986 | CD 56 GGC>CGC | Hb Hamadan | HBB:c.169G>C | β | Causative | β-chain variant | NG_000007.3 | 70893 |
987 | CD 56 GGC>CGC; CD 86 GCC>CCC | Hb Poissy | HBB:c.[169G>C;259G>C] | β | Causative | β-chain variant | NG_000007.3 | 70893 |
988 | CD 56 GGC>GAC (Hb J-Korat , Hb J-Manado , Hb J-Meinung) | Hb J-Bangkok | HBB:c.170G>A | β | Causative | β-chain variant | NG_000007.3 | 70894 |
989 | CD 56-60 (-12bp) | Hb Tochigi | HBB:c.170_181del | β | Causative | β-chain variant | NG_000007.3 | 70894 |
990 | CD 57 AAC>CAC [Asn>His] | Hb Sidcup | HBB:c.172A>C | β | Causative | β-chain variant | NG_000007.3 | 70896 |
991 | CD 57 AAC>GAC | Hb J-Daloa | HBB:c.172A>G | β | Causative | β-chain variant | NG_000007.3 | 70896 |
992 | CD 57 AAC>ACC [Asn>Thr] | Hb Viseu | HBB:c.173A>C | β | Causative | β-chain variant | NG_000007.3 | 70897 |
2333 | CD 57 AAC>AGC [Asn>Ser] | Hb Cork | HBB:c.173A>G | β | Causative | β-chain variant | NG_000007.3 | 70897 |
993 | CD 57 AAC>AAA or AAG | Hb G-Ferrara | HBB:c.174C>A | HBB:c.174C>G | β | Causative | β-chain variant | NG_000007.3 | 70898 |
994 | CD 58 CCT>CAT [Pro>His] | Hb Sheffield | HBB:c.176C>A | β | Causative | β-chain variant | NG_000007.3 | 70900 |
995 | CD 58 CCT>CGT [Pro>Arg] | Hb Dhofar | HBB:c.176C>G | β | Causative | β-chain variant | NG_000007.3 | 70900 |
996 | CD 59 AAG>GAG | Hb I-High Wycombe | HBB:c.178A>G | β | Causative | β-chain variant | NG_000007.3 | 70902 |
2998 | CD 59 AAG>CAG [ Lys>Gln] | Hb Hillsborought | HBB:c.178A>C | β | Causative | β-chain variant | NG_000007.3 | 70902 |
997 | CD 59 AAG>ACG [Lys>Thr] | Hb J-Kaohsiung | HBB:c.179A>C | β | Causative | β-chain variant | NG_000007.3 | 70903 |
3747 | CD 59 AAG>ATG [Lys>Met] | Hb Dahua | HBB:c.179A>T | β | Causative | β-chain variant | NG_000007.3 | 70903 |
998 | CD 59 AAG>AAC or AAT | Hb J-Lome | HBB:c.180G>C | HBB:c.180G>T | β | Causative | β-chain variant | NG_000007.3 | 70904 |
999 | CD 60 GTG>CTG [Val>Leu] | Hb Yatsushiro | HBB:c.181G>C | β | Causative | β-chain variant | NG_000007.3 | 70905 |
1000 | CD 60 GTG>GCG [Leu>Ala] | Hb Collingwood | HBB:c.182T>C | β | Causative | β-chain variant | NG_000007.3 | 70906 |
3298 | CD 60-61 (-6bp): (-TGAAGG) | Hb Tavapy | HBB:c.182_187delTGAAGG | β | Causative | β-chain variant | NG_000007.3 | 70906 |
1002 | CD 61 AAG>CAG | Hb Pocos de Caldas | HBB:c.184A>C | β | Causative | β-chain variant | NG_000007.3 | 70908 |
1003 | CD 61 AAG>GAG | Hb N-Seattle | HBB:c.184A>G | β | Causative | β-chain variant | NG_000007.3 | 70908 |
1004 | CD 61 AAG>ATG | Hb Bologna | HBB:c.185A>T | β | Causative | β-chain variant | NG_000007.3 | 70909 |
1005 | CD 61 AAG>AAC or AAT [Lys>Asn] | Hb Hikari | HBB:c.186G>C | HBB:c.186G>T | β | Causative | β-chain variant | NG_000007.3 | 70910 |
1006 | CD 62 GCT>CCT | Hb Duarte | HBB:c.187G>C | β | Causative | β-chain variant | NG_000007.3 | 70911 |
1007 | CD 62 GCT>GAT | Hb J-Europa | HBB:c.188C>A | β | Causative | β-chain variant | NG_000007.3 | 70912 |
3342 | CD 62 GCT>GTT [Ala>Val] | Hb Hachioji | HBB:c.188C>T | β | Causative | β-chain variant | NG_000007.3 | 70912 |
1008 | CD 63 CAT>AAT [His>Asn] | Hb Haná | HBB:c.190C>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70914 |
1009 | CD 63 CAT>TAT (Hb Hörlein-Weber, Hb Leipzig, Hb M-Arhus, Hb M-Chicago, Hb M-Emory, Hb M-Erlangen, Hb M-Hamburg, Hb M-Hida, Hb M-Kurume, Hb M-Radom, Hb Novi Sad) | Hb M-Saskatoon | HBB:c.190C>T | β | Causative | β-chain variant | NG_000007.3 | 70914 |
1010 | CD 63 CAT>CCT | Hb Bicêtre | HBB:c.191A>C | β | Causative | β-chain variant | NG_000007.3 | 70915 |
1011 | CD 63 CAT>CGT [His>Arg] (Hb Zurich) | Hb Zürich | HBB:c.191A>G | β | Causative | β-chain variant | NG_000007.3 | 70915 |
2456 | CD 63 CAT>CTT [His>Leu] | Hb Temple Street | HBB:c.191A>T | β | Causative | β-chain variant | NG_000007.3 | 70915 |
3629 | CD 64 GGC>AGC [Gly>Ser] | Hb Hezhou | HBB:c.193G>A | β | Causative | β-chain variant | NG_000007.3 | 70917 |
1012 | CD 64 GGC>GCC | Hb Aubagne | HBB:c.194G>C | β | Causative | β-chain variant | NG_000007.3 | 70918 |
1013 | CD 64 GGC>GAC | Hb J-Calabria | HBB:c.194G>A | β | Causative | β-chain variant | NG_000007.3 | 70918 |
1014 | CD 65 AAG>CAG | Hb J-Cairo | HBB:c.196A>C | β | Causative | β-chain variant | NG_000007.3 | 70920 |
3559 | CD 65 AAG>GAG [Lys>Glu] | Hb Guangxi | HBB:c.196A>G | β | Causative | β-chain variant | NG_000007.3 | 70920 |
1016 | CD 65 AAG>ATG | Hb J-Antakya | HBB:c.197A>T | β | Causative | β-chain variant | NG_000007.3 | 70921 |
1017 | CD 65 AAG>AAC or AAT | Hb J-Sicilia | HBB:c.198G>C | HBB:c.198G>T | β | Causative | β-chain variant | NG_000007.3 | 70922 |
1018 | CD 66 AAA>GAA | Hb I-Toulouse | HBB:c.199A>G | β | Causative | β-chain variant | NG_000007.3 | 70923 |
2525 | CD 68/69 (+AAAGTGCTC) | Hb Bronx | HBB:c.199_207dupAAAGTGCTC | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70923 |
1019 | CD 66 AAA>ACA | Hb Chico | HBB:c.200A>C | β | Causative | β-chain variant | NG_000007.3 | 70924 |
3367 | CD 66 AAA>ATA [Lys>Ile] | Hb Vigo | HBB:c.200A>T | β | Causative | β-chain variant | NG_000007.3 | 70924 |
1020 | CD 66 AAA>AAT | Hb Ulm | HBB:c.201A>T | β | Causative | β-chain variant | NG_000007.3 | 70925 |
1021 | CD 67 GTG>ATG [Val>Met] (Hb Bristol-Alesha, Hb Bristol) | Hb Alesha | HBB:c.202G>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70926 |
1023 | CD 67 GTG>GGG [Val>Gly] | Hb Manukau | HBB:c.203T>G | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70927 |
1024 | CD 67 GTG>GAG | Hb M-Milwaukee-I | HBB:c.203T>A | β | Causative | β-chain variant | NG_000007.3 | 70927 |
1025 | CD 67 GTG>GCG | Hb Sydney | HBB:c.203T>C | β | Causative | β-chain variant | NG_000007.3 | 70927 |
1029 | CD 69 (+GCTCGG) | Hb Nishinomiya | HBB:c.204_209dupGCTCGG | β | Causative | β-chain variant | NG_000007.3 | 70928 |
1026 | CD 68 CTC>TTC | Hb Loves Park | HBB:c.205C>T | β | Causative | β-chain variant | NG_000007.3 | 70929 |
1027 | CD 68 CTC>CAC | Hb Brisbane | HBB:c.206T>A | β | Causative | β-chain variant | NG_000007.3 | 70930 |
1028 | CD 68 CTC>CCC [Leu>Pro] | Hb Mizuho | HBB:c.206T>C | β | Causative | β-chain variant | NG_000007.3 | 70930 |
1030 | CD 69 GGT>AGT | Hb City of Hope | HBB:c.208G>A | β | Causative | β-chain variant | NG_000007.3 | 70932 |
1031 | CD 69 GGT>CGT | Hb Kenitra | HBB:c.208G>C | β | Causative | β-chain variant | NG_000007.3 | 70932 |
3798 | CD 69 GGT>TGT [Gly>Cys] | Hb Miguel Servet | HBB:c.208G>T | β | Causative | β-chain variant | NG_000007.3 | 70932 |
1032 | CD 69 GGT>GAT | Hb Rambam | HBB:c.209G>A | β | Causative | β-chain variant | NG_000007.3 | 70933 |
1033 | CD 70 GCC>CCC [Ala>Pro] | Hb Abington | HBB:c.211G>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70935 |
3799 | CD 70 GCC>ACC [Ala>Thr] | Hb La Mesa | HBB:c.211G>A | β | Causative | β-chain variant | NG_000007.3 | 70935 |
1034 | CD 70 GCC>GAC | Hb Seattle | HBB:c.212C>A | β | Causative | β-chain variant | NG_000007.3 | 70936 |
1035 | CD 70 GCC>GGC [Ala>Gly] | Hb Hershey | HBB:c.212C>G | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70936 |
1036 | CD 70 GCC>GTC | Hb Marineo | HBB:c.212C>T | β | Causative | β-chain variant | NG_000007.3 | 70936 |
1037 | CD 71 TTT>TCT | Hb Christchurch | HBB:c.215T>C | β | Causative | β-chain variant | NG_000007.3 | 70939 |
2969 | CD 71 TTT>TAT [Phe>Tyr] | Hb Saint-Clair | HBB:c.215T>A | β | Causative | β-chain variant | NG_000007.3 | 70939 |
2401 | CD 72 AGT>ACT [Ser>Thr] | Hb Phimai | HBB:c.218G>C | β | Causative | β-chain variant | NG_000007.3 | 70942 |
1038 | CD 72 AGT>AGA | Hb Headington | HBB:c.219T>A | β | Causative | β-chain variant | NG_000007.3 | 70943 |
1039 | CD 73 GAT>TAT | Hb Vancouver | HBB:c.220G>T | β | Causative | β-chain variant | NG_000007.3 | 70944 |
1040 | CD 73 GAT>AAT (Hb Korle-Bu) | Hb G-Accra | HBB:c.220G>A | β | Causative | β-chain variant | NG_000007.3 | 70944 |
1043 | CD 73-75 (-GATGGCCTG; + Ala-Arg-Cys-Gln) | Hb Montreal | HBB:c.220_228delinsGCTCGGTGCCAG | β | Causative | β-chain variant | NG_000007.3 | 70944 |
2478 | CD 73 GAT>TAT>TTT [Asp>Phe] | Hb Meylan | HBB:c.[220G>T ;221A>T] | β | Causative | β-chain variant | NG_000007.3 | 70944 |
1041 | CD 73 GAT>GGT | Hb Tilburg | HBB:c.221A>G | β | Causative | β-chain variant | NG_000007.3 | 70945 |
1042 | CD 73 GAT>GTT | Hb Mobile | HBB:c.221A>T | β | Causative | β-chain variant | NG_000007.3 | 70945 |
1045 | CD 74 GGC>AGC [Gly>Ser] | Hb Kokomo | HBB:c.223G>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70947 |
1046 | CD 74 GGC>CGC [Gly>Arg] | Hb Aalborg | HBB:c.223G>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70947 |
1044 | CD 74-76 (-GCCTGG) | Hb Saint-Antoine | HBB:c.224_229delGCCTGG | β | Causative | β-chain variant | NG_000007.3 | 70948 |
1047 | CD 74 GGC>GTC | Hb Bushwick | HBB:c.224G>T | β | Causative | β-chain variant | NG_000007.3 | 70948 |
1048 | CD 74 GGC>GAC | Hb Shepherds Bush | HBB:c.224G>A | β | Causative | β-chain variant | NG_000007.3 | 70948 |
1049 | CD 75 (-CTG) | Hb Vicksburg | HBB:c.226_228delCTG | β | Causative | β-chain variant | NG_000007.3 | 70950 |
1050 | CD 75 CTG>CCG; CD 141 (-CTG) | Hb Atlanta-Coventry | HBB:c.[227T>C;424_426delCTG] | β | Causative | β-chain variant | NG_000007.3 | 70951 |
1051 | CD 75 CTG>CCG | Hb Atlanta | HBB:c.227T>C | β | Causative | β-chain variant | NG_000007.3 | 70951 |
1052 | CD 75 CTG>CGG | Hb Pasadena | HBB:c.227T>G | β | Causative | β-chain variant | NG_000007.3 | 70951 |
4080 | CD 75 CTG>CAG [Leu>Gln] | Hb Raklev | HBB:c.227T>A | β | Causative | β-chain variant | NG_000007.3 | 70951 |
1053 | CD 76 GCT>CCT | Hb Calais | HBB:c.229G>C | β | Causative | β-chain variant | NG_000007.3 | 70953 |
1054 | CD 76 GCT>GTT [Ala>Val] | Hb Harlequin | HBB:c.230C>T | β | Causative | β-chain variant | NG_000007.3 | 70954 |
1055 | CD 76 GCT>GAT | Hb J-Chicago | HBB:c.230C>A | β | Causative | β-chain variant | NG_000007.3 | 70954 |
1056 | CD 77 CAC>TAC; CD 80 AAC>AGC | Hb Villeparisis | HBB:c.[232C>T;242A>G] | β | Causative | β-chain variant | NG_000007.3 | 70956 |
1057 | CD 77 CAC>TAC | Hb Fukuyama | HBB:c.232C>T | β | Causative | β-chain variant | NG_000007.3 | 70956 |
1058 | CD 77 CAC>GAC | Hb J-Iran | HBB:c.232C>G | β | Causative | β-chain variant | NG_000007.3 | 70956 |
2405 | CD 77 CAC>AAC [His>Asn] | Hb Heilbronn | HBB:c.232C>A | β | Causative | β-chain variant | NG_000007.3 | 70956 |
1059 | CD 77 CAC>CTC [His>Leu] | Hb St. Joseph's | HBB:c.233A>T | β | Causative | β-chain variant | NG_000007.3 | 70957 |
1060 | CD 77 CAC>CGC [His>Arg] | Hb Costa Rica | HBB:c.233A>G | β | Causative | β-chain variant | NG_000007.3 | 70957 |
2533 | CD 77 CAC>CCC [His>Pro] | Hb Brooklyn | HBB:c.233A>C | β | Causative | β-chain variant | NG_000007.3 | 70957 |
1061 | CD 77 CAC>CAG | Hb Vienna | HBB:c.234C>G | β | Causative | β-chain variant | NG_000007.3 | 70958 |
2422 | CD 78 CTG>GTG [Leu>Val] | Hb Ullevaal | HBB:c.235C>G | β | Causative | β-chain variant | NG_000007.3 | 70959 |
1062 | CD 78 CTG>CGG | Hb Quin-Hai | HBB:c.236T>G | β | Causative | β-chain variant | NG_000007.3 | 70960 |
3371 | CD 78 CTG>CCG [Leu>Pro] | Hb Penang | HBB:c.236T>C | β | Causative | β-chain variant | NG_000007.3 | 70960 |
1063 | CD 79 GAC>CAC | Hb Tigraye | HBB:c.238G>C | β | Causative | β-chain variant | NG_000007.3 | 70962 |
1064 | CD 79 GAC>AAC | Hb Yaizu | HBB:c.238G>A | β | Causative | β-chain variant | NG_000007.3 | 70962 |
1065 | CD 79 GAC>TAC | Hb Tampa | HBB:c.238G>T | β | Causative | β-chain variant | NG_000007.3 | 70962 |
1066 | CD 79 GAC>GGC [Asp>Gly] | Hb G-Hsi-Tsou | HBB:c.239A>G | β | Causative | β-chain variant | NG_000007.3 | 70963 |
3310 | CD 79 GAC>GCC [Asp>Ala] | Hb Torbay | HBB:c.239A>C | β | Causative | β-chain variant | NG_000007.3 | 70963 |
3919 | CD 79 GAC>GAA [Asp>Glu] | Hb Kalundborg | HBB:c.240C>A | β | Causative | β-chain variant | NG_000007.3 | 70964 |
1067 | CD 80 AAC>TAC [Asn>Tyr] | Hb Hounslow | HBB:c.241A>T | β | Causative | β-chain variant | NG_000007.3 | 70965 |
2307 | CD 80 AAC>CAC [Asn>His] | Hb East Timor | HBB:c.241A>C | β | Causative | β-chain variant | NG_000007.3 | 70965 |
2391 | CD 80 AAC>GAC [Asn>Asp] | Hb Valley Park | HBB:c.241A>G | β | Causative | β-chain variant | NG_000007.3 | 70965 |
2445 | CD 80 -AAC [-Asn] | Hb Saint-Chamond | HBB:c.241_243delAAC | β | Causative | β-chain variant | NG_000007.3 | 70965 |
3392 | CD 80 AAC>AGC [Asn>Ser] | Hb Moncloa | HBB:c.242A>G | β | Causative | β-chain variant | NG_000007.3 | 70966 |
1068 | CD 80 AAC>AAG [Asn>Lys] (Hb Gifu) | Hb G-Szuhu | HBB:c.243C>G | β | Causative | β-chain variant | NG_000007.3 | 70967 |
2443 | CD 81 CTC>TTC [Leu>Phe] | Hb Seville | HBB:c.244C>T | β | Causative | β-chain variant | NG_000007.3 | 70968 |
1069 | CD 81 CTC>CGC | Hb Baylor | HBB:c.245T>G | β | Causative | β-chain variant | NG_000007.3 | 70969 |
1070 | CD 81 CTC>CAC | Hb La Roche-sur-Yon | HBB:c.245T>A | β | Causative | β-chain variant | NG_000007.3 | 70969 |
1071 | CD 82 AAG>CAG | Hb Tsurumai | HBB:c.247A>C | β | Causative | β-chain variant | NG_000007.3 | 70971 |
1072 | CD 82 AAG>GAG | Hb Gàmbara | HBB:c.247A>G | β | Causative | β-chain variant | NG_000007.3 | 70971 |
1073 | CD 82 AAG>ACG | Hb Rahere | HBB:c.248A>C | β | Causative | β-chain variant | NG_000007.3 | 70972 |
1074 | CD 82 AAG>ATG | Hb Helsinki | HBB:c.248A>T | β | Causative | β-chain variant | NG_000007.3 | 70972 |
1075 | CD 82 AAG>AGG | Hb Taradale | HBB:c.248A>G | β | Causative | β-chain variant | NG_000007.3 | 70972 |
1076 | CD 82 AAG>AAC | Hb Providence | HBB:c.249G>C | β | Causative | β-chain variant | NG_000007.3 | 70973 |
1077 | CD 83 GGC>CGC [Gly>Arg] | Hb Muskegon | HBB:c.250G>C | β | Causative | β-chain variant | NG_000007.3 | 70974 |
1078 | CD 83 GGC>TGC [Gly>Cys] | Hb Ta-Li | HBB:c.250G>T | β | Causative | β-chain variant | NG_000007.3 | 70974 |
2534 | CD 83 GGC>AGC [Gly>Ser] | Hb Basking Ridge | HBB:c.250G>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70974 |
1079 | CD 83 GGC>GAC | Hb Pyrgos | HBB:c.251G>A | β | Causative | β-chain variant | NG_000007.3 | 70975 |
1080 | CD 84 ACC>GCC | Hb Saale | HBB:c.253A>G | β | Causative | β-chain variant | NG_000007.3 | 70977 |
1081 | CD 84 ACC>AAC [Thr>Asn] | Hb Beaujolais | HBB:c.254C>A | β | Causative | β-chain variant | NG_000007.3 | 70978 |
1082 | CD 84 ACC>ATC | Hb Kofu | HBB:c.254C>T | β | Causative | β-chain variant | NG_000007.3 | 70978 |
3965 | CD 84-87 (-CTTTGCCACA) (+TTTTTCTCAG) (Hb Donguan-Dongcheng) | Hb Wanjiang | HBB:c.255_264delinsTTTTTCTCAG | β | Causative | β-chain variant | NG_000007.3 | 70979 |
3323 | CD 85 TTT>CTT [Phe>Leu] | Hb San Martin | HBB:c.256T>C | β | Causative | β-chain variant | NG_000007.3 | 70980 |
1083 | CD 85 TTT>TCT (Hb Bryn Mawr) | Hb Buenos Aires | HBB:c.257T>C | β | Causative | β-chain variant | NG_000007.3 | 70981 |
2975 | CD 85 TTT>TGT [Phe>Cys] | Hb Grantham | HBB:c.257T>G | β | Causative | β-chain variant | NG_000007.3 | 70981 |
3586 | CD 85 TTT>TTG [Phe>Leu] | Hb Kennisis | HBB:c.258T>G | β | Causative | β-chain variant | NG_000007.3 | 70982 |
1084 | CD 86 GCC>CCC | Hb Cardarelli | HBB:c.259G>C | β | Causative | β-chain variant | NG_000007.3 | 70983 |
1085 | CD 86 GCC>ACC>ATC [Ala>Ile] | Hb Nebraska | HBB:c.[259G>A;260C>T] | β | Causative | β-chain variant | NG_000007.3 | 70983 |
3065 | CD 86 GCC>ACC [Ala>Thr] | Hb Seoul | HBB:c.259G>A | β | Causative | β-chain variant | NG_000007.3 | 70983 |
1086 | CD 86 GCC>GAC | Hb Olomouc | HBB:c.260C>A | β | Causative | β-chain variant | NG_000007.3 | 70984 |
2454 | CD 86 GCC>GTC [Ala>Val] | Hb Izmir | HBB:c.260C>T | β | Causative | β-chain variant | NG_000007.3 | 70984 |
1087 | CD 87 (-ACA) | Hb Tours | HBB:c.262_264delACA | β | Causative | β-chain variant | NG_000007.3 | 70986 |
1088 | CD 87 ACA>CCA | Hb Valletta | HBB:c.262A>C | β | Causative | β-chain variant | NG_000007.3 | 70986 |
1089 | CD 87 ACA>ATA | Hb Quebec-Chori | HBB:c.263C>T | β | Causative | β-chain variant | NG_000007.3 | 70987 |
1090 | CD 87 ACA>AAA | Hb D-Ibadan | HBB:c.263C>A | β | Causative | β-chain variant | NG_000007.3 | 70987 |
3377 | CD 87 ACA>AGA [Thr>Arg] | Hb Saint Jean d Ardieres | HBB:c.263C>G | β | Causative | β-chain variant | NG_000007.3 | 70987 |
1091 | CD 88 CTG>GTG [Leu>Val] | Hb Oofuna | HBB:c.265C>G | β | Causative | β-chain variant | NG_000007.3 | 70989 |
3009 | CD 88 CTG>ATG [Leu>Met] | Hb NISER | HBB:c.265C>A | β | Causative | β-chain variant | NG_000007.3 | 70989 |
1092 | CD 88 CTG>CGG | Hb Borås | HBB:c.266T>G | β | Causative | β-chain variant | NG_000007.3 | 70990 |
1093 | CD 88 CTG>CCG | Hb Santa Ana | HBB:c.266T>C | β | Causative | β-chain variant | NG_000007.3 | 70990 |
1095 | CD 89 AGT>AAT | Hb Créteil | HBB:c.269G>A | β | Causative | β-chain variant | NG_000007.3 | 70993 |
1096 | CD 89 AGT>ACT | Hb Villaverde | HBB:c.269G>C | β | Causative | β-chain variant | NG_000007.3 | 70993 |
1094 | CD 89 AGT>AGR [Ser>Arg] | Hb Vanderbilt | HBB:c.270T>R | β | Causative | β-chain variant | NG_000007.3 | 70994 |
2965 | CD 89-90 (-TGAG) | Hb Wilde | HBB:c.270_273delTGAG | β | Causative | β-chain variant | NG_000007.3 | 70994 |
1097 | CD 90 GAG>AAG | Hb Agenogi | HBB:c.271G>A | β | Causative | β-chain variant | NG_000007.3 | 70995 |
1118 | CD 94/95 +15 bp [+Glu-Leu-His-Cys-Asp] | Hb Fairfax | HBB:c.271_285dupGAGCTGCACTGTGAC | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 70995 |
2491 | CD 90 GAG>CAG [Glu>Gln] | Hb Henan | HBB:c.271G>C | β | Causative | β-chain variant | NG_000007.3 | 70995 |
1098 | CD 90 GAG>GGG | Hb Roseau-Pointe a Pitre | HBB:c.272A>G | β | Causative | β-chain variant | NG_000007.3 | 70996 |
3593 | CD 90 GAG>GCG [Glu>Ala] | Hb Shenzhen | HBB:c.272A>C | β | Causative | β-chain variant | NG_000007.3 | 70996 |
1099 | CD 90 GAG>GAC [Glu>Asp] | Hb Pierre-Bénite | HBB:c.273G>C | β | Causative | β-chain variant | NG_000007.3 | 70997 |
1124 | CD 95/96 (+15 bp) | Hb Koriyama | HBB:c.274_288dup | β | Causative | β-chain variant | NG_000007.3 | 70998 |
1101 | CD 91 CTG>CCG | Hb Sabine | HBB:c.275T>C | β | Causative | β-chain variant | NG_000007.3 | 70999 |
1102 | CD 91 CTG>CGG | Hb Caribbean | HBB:c.275T>G | β | Causative | β-chain variant | NG_000007.3 | 70999 |
1103 | CD 92 CAC>GAC | Hb J-Altgeld Gardens | HBB:c.277C>G | β | Causative | β-chain variant | NG_000007.3 | 71001 |
1104 | CD 92 CAC>TAC (Hb M-Akita, Hb M-Hyde Park) | Hb M-Milwaukee-2 | HBB:c.277C>T | β | Causative | β-chain variant | NG_000007.3 | 71001 |
1105 | CD 92 CAC>AAC | Hb Redondo | HBB:c.277C>A | β | Causative | β-chain variant | NG_000007.3 | 71001 |
1106 | CD 92 CAC>CCC | Hb Newcastle | HBB:c.278A>C | β | Causative | β-chain variant | NG_000007.3 | 71002 |
1107 | CD 92 CAC>CGC | Hb Mozhaisk | HBB:c.278A>G | β | Causative | β-chain variant | NG_000007.3 | 71002 |
1108 | CD 92 CAC>CCC; CD 104 AGG>AGC | Hb Duino | HBB:c.[278A>C;315G>C] | β | Causative | β-chain variant | NG_000007.3 | 71002, 71039 |
1109 | CD 92 CAC>CAG [His>Gln] (Hb Istanbul) | Hb Saint Etienne | HBB:c.279C>G | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71003 |
1100 | CD 93-97 (-15 bp) | Hb Gun Hill | Hb GH | HBB:c.280_294delTGTGACAAGCTGCAC | β | Causative | β-chain variant | NG_000007.3 | 71004 |
1110 | CD 93 TGT>CGT: CD 121 GAA>CAA | Hb Cleveland | HBB:c.[280T>C;364G>C] | β | Causative | β-chain variant | NG_000007.3 | 71004 |
1111 | CD 93 TGT>CGT | Hb Okazaki | HBB:c.280T>C | β | Causative | β-chain variant | NG_000007.3 | 71004 |
1112 | CD 93 TGT>TAT | Hb Fort Dodge | HBB:c.281G>A | β | Causative | β-chain variant | NG_000007.3 | 71005 |
2442 | CD 93 TGT>TCT [Cys>Ser] | Hb Riesa | HBB:c.281G>C | β | Causative | β-chain variant | NG_000007.3 | 71005 |
2441 | CD 93 TGT>TGG [Cys>Trp] | Hb Santa Giusta Sardegna | HBB:c.282T>G | β | Causative | β-chain variant | NG_000007.3 | 71006 |
1114 | CD 94 GAC>TAC | Hb Geldrop St Anna | HBB:c.283G>T | β | Causative | β-chain variant | NG_000007.3 | 71007 |
1115 | CD 94 GAC>CAC | Hb Barcelona | HBB:c.283G>C | β | Causative | β-chain variant | NG_000007.3 | 71007 |
1116 | CD 94 GAC>AAC | Hb Bunbury | HBB:c.283G>A | β | Causative | β-chain variant | NG_000007.3 | 71007 |
1117 | CD 94 GAC>GGC | Hb Chandigarh | HBB:c.284A>G | β | Causative | β-chain variant | NG_000007.3 | 71008 |
1119 | CD 95 AAG>GAG (Hb Hopkins-I, Hb Jenkins, Hb N-Memphis, Hb Kenwood) | Hb N-Baltimore | HBB:c.286A>G | β | Causative | β-chain variant | NG_000007.3 | 71010 |
2545 | CD 95 AAG>CAG [Lys>Gln] | Hb J-Valencia | HBB:c.286A>C | β | Causative | β-chain variant | NG_000007.3 | 71010 |
1120 | CD 95 AAG>ATG | Hb J-Cordoba | HBB:c.287A>T | β | Causative | β-chain variant | NG_000007.3 | 71011 |
1121 | CD 95 AAG>AAY [Lys>Asn] | Hb Detroit | HBB:c.288G>Y | β | Causative | β-chain variant | NG_000007.3 | 71012 |
1122 | CD 96 CTG>GTG | Hb Regina | HBB:c.289C>G | β | Causative | β-chain variant | NG_000007.3 | 71013 |
1123 | CD 96 CTG>CCG | Hb Debrousse | HBB:c.290T>C | β | Causative | β-chain variant | NG_000007.3 | 71014 |
3876 | CD 96 CTG>CGG [Leu>Arg] | Hb Laibin | HBB:c.290T>G | β | Causative | β-chain variant | NG_000007.3 | 71014 |
1126 | CD 97 CAC>TAC | Hb Moriguchi | HBB:c.292C>T | β | Causative | β-chain variant | NG_000007.3 | 71016 |
1127 | CD 97 CAC>AAC | Hb Santa Clara | HBB:c.292C>A | β | Causative | β-chain variant | NG_000007.3 | 71016 |
1125 | CD 97/98 (-ACG) | Hb Galicia | HBB:c.293_295delACG | β | Causative | β-chain variant | NG_000007.3 | 71017 |
1128 | CD 97 CAC>CTC | Hb Wood | HBB:c.293A>T | β | Causative | β-chain variant | NG_000007.3 | 71017 |
1129 | CD 97 CAC>CCC | Hb Nagoya | HBB:c.293A>C | β | Causative | β-chain variant | NG_000007.3 | 71017 |
1130 | CD 97 CAC>CAA, also CAC>CAG | Hb Malmö | HBB:c.294C>A | HBB:c.294C>G | β | Causative | β-chain variant | NG_000007.3 | 71018 |
1131 | CD 98 GTG>ATG [Val>Met] (Hb San Francisco (Pacific), Hb Ube-1) | Hb Köln | HBB:c.295G>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71019 |
2413 | CD 98 GTG>CTG [Val>Leu] | Hb Phou Bia | HBB:c.295G>C | β | Causative | β-chain variant | NG_000007.3 | 71019 |
1132 | CD 98 GTG>GGG | Hb Nottingham | HBB:c.296T>G | β | Causative | β-chain variant | NG_000007.3 | 71020 |
1133 | CD 98 GTG>GAG [Val>Glu] | Hb Mainz | HBB:c.296T>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71020 |
1134 | CD 98 GTG>GCG | Hb Djelfa | HBB:c.296T>C | β | Causative | β-chain variant | NG_000007.3 | 71020 |
2966 | CD 98/99 (+TG) | Hb Patagonia | HBB:c.296_297dup | β | Causative | β-chain variant | NG_000007.3 | 71020 |
1135 | CD 99 GAT>TAT | Hb Ypsilanti | HBB:c.298G>T | β | Causative | β-chain variant | NG_000007.3 | 71022 |
1136 | CD 99 GAT>CAT | Hb Yakima | HBB:c.298G>C | β | Causative | β-chain variant | NG_000007.3 | 71022 |
1137 | CD 99 GAT>AAT | Hb Kempsey | HBB:c.298G>A | β | Causative | β-chain variant | NG_000007.3 | 71022 |
1138 | CD 99 GAT>GGT | Hb Hotel-Dieu | HBB:c.299A>G | β | Causative | β-chain variant | NG_000007.3 | 71023 |
1139 | CD 99 GAT>GCT | Hb Radcliffe | HBB:c.299A>C | β | Causative | β-chain variant | NG_000007.3 | 71023 |
1140 | CD 99 GAT>GTT | Hb Chemilly | HBB:c.299A>T | β | Causative | β-chain variant | NG_000007.3 | 71023 |
1141 | CD 99 GAT>GAA [Asp>Glu] | Hb Coimbra | HBB:c.300T>A | β | Causative | β-chain variant | NG_000007.3 | 71024 |
1142 | CD 100 CCT>GCT [Pro>Ala] | Hb Nice | HBB:c.301C>G | β | Causative | β-chain variant | NG_000007.3 | 71025 |
2399 | CD 100 CCT>ACT [Pro>Thr] | Hb Bellevue II | HBB:c.301C>A | β | Causative | β-chain variant | NG_000007.3 | 71025 |
2412 | CD 100 CCT>TCT [Pro>Ser] | Hb Niort | HBB:c.301C>T | β | Causative | β-chain variant | NG_000007.3 | 71025 |
1143 | CD 100 CCT>CGT | Hb New Mexico | HBB:c.302C>G | β | Causative | β-chain variant | NG_000007.3 | 71026 |
1144 | CD 100 CCT>CTT | Hb Brigham | HBB:c.302C>T | β | Causative | β-chain variant | NG_000007.3 | 71026 |
1145 | CD 101 GAG>CAG | Hb Rush | HBB:c.304G>C | β | Causative | β-chain variant | NG_000007.3 | 71028 |
1146 | CD 101 GAG>AAG | Hb British Columbia | HBB:c.304G>A | β | Causative | β-chain variant | NG_000007.3 | 71028 |
1147 | CD 101 GAG>GGG | Hb Alberta | HBB:c.305A>G | β | Causative | β-chain variant | NG_000007.3 | 71029 |
1148 | CD 101 GAG>GCG | Hb Youngstown | Hb St Mary's | HBB:c.305A>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71029 |
2432 | CD 101 GAG>GTG [Glu>Val] | Hb Belfort | HBB:c.305A>T | β | Causative | β-chain variant | NG_000007.3 | 71029 |
1149 | CD 101 GAG>GAC or GAT | Hb Potomac | HBB:c.306G>C | HBB:c.306G>T | β | Causative | β-chain variant | NG_000007.3 | 71030 |
1150 | CD 102 AAC>TAC | Hb Saint Mandé | HBB:c.307A>T | β | Causative | β-chain variant | NG_000007.3 | 71031 |
1151 | CD 102 AAC>CAC [Asn>His] | Hb Canebiere | HBB:c.307A>C | β | Causative | β-chain variant | NG_000007.3 | 71031 |
1152 | CD 102 AAC>AGC | Hb Beth Israel | HBB:c.308A>G | β | Causative | β-chain variant | NG_000007.3 | 71032 |
1153 | CD 102 AAC>ACC [Asn>Thr] (Hb Reissmann) | Hb Kansas | HBB:c.308A>C | β | Causative | β-chain variant | NG_000007.3 | 71032 |
1154 | CD 102 AAC>AAA or AAG | Hb Richmond | HBB:c.309C>A | HBB:c.309C>G | β | Causative | β-chain variant | NG_000007.3 | 71033 |
1155 | CD 103 TTC>GTC | Hb Sparta | HBB:c.310T>G | β | Causative | β-chain variant | NG_000007.3 | 71034 |
1156 | CD 103 TTC>ATC | Hb Saint Nazaire | HBB:c.310T>A | β | Causative | β-chain variant | NG_000007.3 | 71034 |
3385 | CD 103 TTC>TAC [Phe>Tyr] | Hb Gavle | HBB:c.311T>A | β | Causative | β-chain variant | NG_000007.3 | 71035 |
4114 | CD 103 TTC>TCC [Phe>Ser] | Hb Koskullskulle | HBB:c.311T>C | β | Causative | β-chain variant | NG_000007.3 | 71035 |
1157 | CD 103 TTC>TTG | Hb Heathrow | HBB:c.312C>G | β | Causative | β-chain variant | NG_000007.3 | 71036 |
1158 | CD 104 AGG>TGG | Hb Sainte Eugénie | HBB:c.313A>T | β | Causative | β-chain variant | NG_000007.3 | 71037 |
2406 | CD 104 AGG>GGG [Arg>Gly] | Hb Nîmes | HBB:c.313A>G | β | Causative | β-chain variant | NG_000007.3 | 71037 |
1159 | CD 104 AGG>ACG | Hb Sherwood Forest | HBB:c.314G>C | β | Causative | β-chain variant | NG_000007.3 | 71038 |
1161 | CD 104 AGG>AAG | Hb Alzette | HBB:c.314G>A | β | Causative | β-chain variant | NG_000007.3 | 71038 |
2411 | CD 104 AGG>ATG [Arg>Met] | Hb Bad Salzuflen | HBB:c.314G>T | β | Causative | β-chain variant | NG_000007.3 | 71038 |
1162 | CD 104 AGG>AGC [Arg>Ser] | Hb Camperdown | HBB:c.315G>C | β | Causative | β-chain variant | NG_000007.3 | 71039 |
1163 | CD 105 CTC>TTC | Hb South Milwaukee | HBB:c.316C>T | β | Causative | β-chain variant | NG_000007.3 | 71890 |
4100 | CD 105 CTC>GTC [Leu>Val] | Hb Odder | HBB:c.316C>G | β | Causative | β-chain variant | NG_000007.3 | 71890 |
2379 | CD 6 GAG>GTG [Glu>Val] AND CD 105 CTC>CCC [Leu>Pro] | Hb S-San Martin | HBB:c.[20A>T ;317T>C] | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71891 |
2404 | CD 105 CTC>CCC [Leu>Pro] | Hb Bellevue IV | HBB:c.317T>C | β | Causative | β-chain variant | NG_000007.3 | 71891 |
1166 | CD 106 CTG>CCG [Leu>Pro] (Hb Casper) | Hb Southampton | HBB:c.320T>C | β | Causative | β-chain variant | NG_000007.3 | 71894 |
1167 | CD 106 CTG>CAG | Hb Tübingen | HBB:c.320T>A | β | Causative | β-chain variant | NG_000007.3 | 71894 |
1168 | CD 107 GGC>CGC | Hb Burke | HBB:c.322G>C | β | Causative | β-chain variant | NG_000007.3 | 71896 |
1169 | CD 107 GGC>GAC | Hb Lulu Island | HBB:c.323G>A | β | Causative | β-chain variant | NG_000007.3 | 71897 |
3309 | CD 107 GGC>GTC [Gly>Val] | Hb Nurnberg | HBB:c.323G>T | β | Causative | β-chain variant | NG_000007.3 | 71897 |
1170 | CD 108 AAC>GAC | Hb Yoshizuka | HBB:c.325A>G | β | Causative | β-chain variant | NG_000007.3 | 71899 |
1171 | CD 108 AAC>CAC [Asn>His] | Hb Shizuoka | HBB:c.325A>C | β | Causative | β-chain variant | NG_000007.3 | 71899 |
1172 | CD 108 AAC>ATC | Hb Schlierbach | HBB:c.326A>T | β | Causative | β-chain variant | NG_000007.3 | 71900 |
1173 | CD 108 AAC>AGC [Asn>Ser] (Hb Serres) | Hb Santa Juana | HBB:c.326A>G | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71900 |
1174 | CD 108 AAC>AAA or AAG | Hb Presbyterian | HBB:c.327C>A | HBB:c.327C>G | β | Causative | β-chain variant | NG_000007.3 | 71901 |
1176 | CD 109 GTG>CTG or TTG | Hb Johnstown | HBB:c.328G>C | HBB:c.328G>T | β | Causative | β-chain variant | NG_000007.3 | 71902 |
1177 | CD 109 GTG>ATG | Hb San Diego | HBB:c.328G>A | β | Causative | β-chain variant | NG_000007.3 | 71902 |
3384 | CD 110 CTG>CGG [Leu>Arg] | Hb London-Ontario | HBB:c.332T>G | β | Causative | β-chain variant | NG_000007.3 | 71906 |
1179 | CD 111 GTC>CTC, CD 119 GGC>GAC | Hb Fannin-Lubbock II | HBB:c.[334G>C;359G>A] | β | Causative | β-chain variant | NG_000007.3 | 71908 |
1180 | CD 111 GTC>TTC [Val>Phe] | Hb Peterborough | HBB:c.334G>T | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71908 |
1181 | CD 111 GTC>GCC [Val>Ala] | Hb Stanmore | HBB:c.335T>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71909 |
3001 | CD 111 GTC>GGC [Val>Gly] | Hb Belluno | HBB:c.335T>G | β | Causative | β-chain variant | NG_000007.3 | 71909 |
1182 | CD 112 TGT>CGT [Cys>Arg] | Hb Indianapolis | HBB:c.337T>C | β | Causative | β-chain variant | NG_000007.3 | 71911 |
2434 | CD 112 TGT>GGT [Cys>Gly] | Hb Saint-Marcellin | HBB:c.337T>G | β | Causative | β-chain variant | NG_000007.3 | 71911 |
1183 | CD 112 TGT>TTT | Hb Canterbury | HBB:c.338G>T | β | Causative | β-chain variant | NG_000007.3 | 71912 |
1184 | CD 112 TGT>TAT | Hb Yahata | HBB:c.338G>A | β | Causative | β-chain variant | NG_000007.3 | 71912 |
1195 | CD 112-116 (+GTGTGCTGGCCC) | Hb Antibes-Juan-Les-Pins | HBB:c.338_349dupGTGTGCTGGCCC | β | Causative | β-chain variant | NG_000007.3 | 71912 |
4105 | CD112 TGT>TCT [Cys>Ser] | Hb Jiangxi | HBB:c.338G>C | β | Causative | β-chain variant | NG_000007.3 | 71912 |
1185 | CD 112 TGT>TGG | Hb Toranomon | HBB:c.339T>G | β | Causative | β-chain variant | NG_000007.3 | 71913 |
1186 | CD 113 GTG>CTG or TTG [Val>Leu] | Hb Champagne | HBB:c.340G>C | HBB:c.340G>T | β | Causative | β-chain variant | NG_000007.3 | 71914 |
1187 | CD 113 GTG>GAG [Val>Glu] (Hb Kaohsiung) | Hb New York | HBB:c.341T>A | β | Causative | β-chain variant | NG_000007.3 | 71915 |
1188 | CD 114 CTG>ATG; CD 119 GGC>GAC | Hb Masuda | HBB:c.[343C>A;359G>A] | β | Causative | β-chain variant | NG_000007.3 | 71917 |
1190 | CD 114 CTG>ATG | Hb Zengcheng | HBB:c.343C>A | β | Causative | β-chain variant | NG_000007.3 | 71917 |
1192 | CD 115 GCC>CCC | Hb Madrid | HBB:c.346G>C | β | Causative | β-chain variant | NG_000007.3 | 71920 |
1193 | CD 115 GCC>GTC [Ala>Val] | Hb Roma | HBB:c.347C>T | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71921 |
1196 | CD 116 CAT>TAT | Hb Rhode Island | HBB:c.349C>T | β | Causative | β-chain variant | NG_000007.3 | 71923 |
1197 | CD 116 CAT>CCT [His>Pro] | Hb Miami | HBB:c.350A>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71924 |
1198 | CD 116 CAT>CGT [His>Ala] | Hb Sfax | HBB:c.350A>G | β | Causative | β-chain variant | NG_000007.3 | 71924 |
1199 | CD 116 CAT>CTT | Hb Vexin | HBB:c.350A>T | β | Causative | β-chain variant | NG_000007.3 | 71924 |
1200 | CD 116 CAT>CAA or CAG | Hb Hafnia | HBB:c.351T>A | HBB:c.351T>G | β | Causative | β-chain variant | NG_000007.3 | 71925 |
1201 | CD 117 CAC>AAC | Hb Brent | HBB:c.352C>A | β | Causative | β-chain variant | NG_000007.3 | 71926 |
1202 | CD 117 CAC>TAC | Hb Tsukumi | HBB:c.352C>T | β | Causative | β-chain variant | NG_000007.3 | 71926 |
1203 | CD 117 CAC>GAC [His>Asp] | Hb North York | HBB:c.352C>G | β | Causative | β-chain variant | NG_000007.3 | 71926 |
1204 | CD 117 CAC>CGC | Hb P-Galveston | HBB:c.353A>G | β | Causative | β-chain variant | NG_000007.3 | 71927 |
1205 | CD 117 CAC>CCC | Hb Saitama | HBB:c.353A>C | β | Causative | β-chain variant | NG_000007.3 | 71927 |
3651 | CD 117 CAC>CAG [His>Gln] | Hb Murcia | HBB:c.354C>G | β | Causative | β-chain variant | NG_000007.3 | 71928 |
1207 | CD 118 TTT>GTT | Hb Sodertalje | HBB:c.355T>G | β | Causative | β-chain variant | NG_000007.3 | 71929 |
1208 | CD 118 TTT>TGT | Hb Harrow | HBB:c.356T>G | β | Causative | β-chain variant | NG_000007.3 | 71930 |
1209 | CD 118 TTT>TAT | Hb Minneapolis-Laos | HBB:c.356T>A | β | Causative | β-chain variant | NG_000007.3 | 71930 |
2334 | CD 118 TTT>TCT [Phe>Ser] | Hb Basingstoke | HBB:c.356T>C | β | Causative | β-chain variant | NG_000007.3 | 71930 |
2410 | CD 119 GGC>CGC [Gly>Arg] | Hb Angouleme | HBB:c.358G>C | β | Causative | β-chain variant | NG_000007.3 | 71932 |
2490 | CD 119 GGC>AGC [Gly>Ser] | Hb Madison-NC | HBB:c.358G>A | β | Causative | β-chain variant | NG_000007.3 | 71932 |
1210 | CD 119 GGC>GAC [Gly>Asp] | Hb Fannin-Lubbock I | HBB:c.359G>A | β | Causative | β-chain variant | NG_000007.3 | 71933 |
1211 | CD 119 GGC>GTC | Hb Bougardirey-Mali | HBB:c.359G>T | β | Causative | β-chain variant | NG_000007.3 | 71933 |
1212 | CD 119 GGC>GCC | Hb Iowa | HBB:c.359G>C | β | Causative | β-chain variant | NG_000007.3 | 71933 |
1213 | CD 120 AAA>GAA | Hb Hijiyama | HBB:c.361A>G | β | Causative | β-chain variant | NG_000007.3 | 71935 |
1214 | CD 120 AAA>CAA | Hb Takamatsu | HBB:c.361A>C | β | Causative | β-chain variant | NG_000007.3 | 71935 |
1215 | CD 120 AAA>ATA | Hb Jianghua | HBB:c.362A>T | β | Causative | β-chain variant | NG_000007.3 | 71936 |
1216 | CD 120 AAA>AAC | Hb Riyadh | HBB:c.363A>C | β | Causative | β-chain variant | NG_000007.3 | 71937 |
2973 | CD 120 AAA>AAT [Lys>Asn] | Hb Belsize Park | HBB:c.363A>T | β | Causative | β-chain variant | NG_000007.3 | 71937 |
1217 | CD 121 GAA>CAA [Glu>Gln] (Hb D-Chicago, Hb D-North Carolina, Hb D-Portugal, Hb D-Los Angeles, Hb Oak Ridge) | Hb D-Punjab | HBB:c.364G>C | β | Causative | β-chain variant | NG_000007.3 | 71938 |
1218 | CD 121 GAA>AAA (Hb Egypt, Hb O-Thrace) | Hb O-Arab | HBB:c.364G>A | β | Causative | β-chain variant | NG_000007.3 | 71938 |
1219 | CD 121 GAA>GCA | Hb D-Neath | HBB:c.365A>C | β | Causative | β-chain variant | NG_000007.3 | 71939 |
1220 | CD 121 GAA>GGA | Hb St. Francis | HBB:c.365A>G | β | Causative | β-chain variant | NG_000007.3 | 71939 |
1221 | CD 121 GAA>GTA | Hb Beograd | HBB:c.365A>T | β | Causative | β-chain variant | NG_000007.3 | 71939 |
3934 | CD 121 GAA>GAC [Glu>Asp] | Hb Westport | HBB:c.366A>C | β | Causative | β-chain variant | NG_000007.3 | 71940 |
1015 | CD 65 AAG>ATG; CD 122 TTC>CTC or TTG or TTA | Hb Casablanca | HBB:c.[367T>C ; 197A>T] | HBB:c.[369C>A ; 197A>T] | HBB:c.[369C>G; 197A>T] | β | Causative | β-chain variant | NG_000007.3 | 71941 |
1222 | CD 122 TTC>CTC or TTG or TTA | Hb Bushey | HBB:c.367T>C | HBB:c.369C>A | HBB:c.369C>G | β | Causative | β-chain variant | NG_000007.3 | 71941 |
1223 | CD 122 TTC>TCC [Phe>Ser] | Hb Caruaru | HBB:c.368T>C | β | Causative | β-chain variant | NG_000007.3 | 71942 |
4022 | CD 122 TTC>TGC [Phe>Cys] | Hb Tanah Merah | HBB:c.368T>G | β | Causative | β-chain variant | NG_000007.3 | 71942 |
1225 | CD 123 ACC>AAC | Hb Ernz | HBB:c.371C>A | β | Causative | β-chain variant | NG_000007.3 | 71945 |
1226 | CD 123 ACC>ATC | Hb Villejuif | HBB:c.371C>T | β | Causative | β-chain variant | NG_000007.3 | 71945 |
1227 | CD 124 CCA>TCA | Hb Tunis | HBB:c.373C>T | β | Causative | β-chain variant | NG_000007.3 | 71947 |
3556 | CD 124 CCA>ACA [Pro>Thr] (Hb Yuxi) | Hb Gibbon | HBB:c.373C>A | β | Causative | β-chain variant | NG_000007.3 | 71947 |
1228 | CD 124 CCA>CAA | Hb Ty Gard | HBB:c.374C>A | β | Causative | β-chain variant | NG_000007.3 | 71948 |
1229 | CD 124 CCA>CTA | Hb Tende | HBB:c.374C>T | β | Causative | β-chain variant | NG_000007.3 | 71948 |
1230 | CD 124 CCA>CGA [Pro>Arg] | Hb Khartoum | HBB:c.374C>G | β | Causative | β-chain variant | NG_000007.3 | 71948 |
3313 | CD 125 CCA>ACA [Pro>Thr] | Hb Novara | HBB:c.376C>A | β | Causative | β-chain variant | NG_000007.3 | 71950 |
1231 | CD 126 GTG>CTG | Hb Molfetta | HBB:c.379G>C | β | Causative | β-chain variant | NG_000007.3 | 71953 |
1233 | CD 126 GTG>GCG | Hb Beirut | HBB:c.380T>C | β | Causative | β-chain variant | NG_000007.3 | 71954 |
1234 | CD 126 GTG>GAG | Hb Hofu | HBB:c.380T>A | β | Causative | β-chain variant | NG_000007.3 | 71954 |
1236 | CD 127 CAG>AAG | Hb Brest | HBB:c.382C>A | β | Causative | β-chain variant | NG_000007.3 | 71956 |
1237 | CD 127 CAG>GAG | Hb Complutense | HBB:c.382C>G | β | Causative | β-chain variant | NG_000007.3 | 71956 |
1242 | CD 128 GCT>GTT | Hb Sitia | HBB:c.386C>T | β | Causative | β-chain variant | NG_000007.3 | 71960 |
1243 | CD 128 GCT>GAT [Ala>Asp] | Hb J-Guantanamo | HBB:c.386C>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71960 |
1244 | CD 129 GCC>CCC | Hb Crete | HBB:c.388G>C | β | Causative | β-chain variant | NG_000007.3 | 71962 |
1245 | CD 129 GCC>GTC [Ala>Val] | Hb La Desirade | HBB:c.389C>T | β | Causative | β-chain variant | NG_000007.3 | 71963 |
1246 | CD 129 GCC>GAC [Ala>Asp] (Hb K-Cameroon) | Hb J-Taichung | HBB:c.389C>A | β | Causative | β-chain variant | NG_000007.3 | 71963 |
3951 | CD 129-133 (-CCTATCAGAAAGT) | Hb Phoenix | HBB:c.389_401del | β | Causative | β-chain variant | NG_000007.3 | 71963 |
1248 | CD 130 TAT>GAT | Hb Wien | HBB:c.391T>G | β | Causative | β-chain variant | NG_000007.3 | 71965 |
1249 | CD 130 TAT>TGT [Tyr>Cys] | Hb Montfermeil | HBB:c.392A>G | β | Causative | β-chain variant | NG_000007.3 | 71966 |
1250 | CD 130 TAT>TCT | Hb Nevers | HBB:c.392A>C | β | Causative | β-chain variant | NG_000007.3 | 71966 |
1251 | CD 131 CAG>GAG | Hb Camden | HBB:c.394C>G | β | Causative | β-chain variant | NG_000007.3 | 71968 |
1252 | CD 131 CAG>AAG | Hb Shelby | HBB:c.394C>A | β | Causative | β-chain variant | NG_000007.3 | 71968 |
1253 | CD 131 CAG>CGG | Hb Sarrebourg | HBB:c.395A>G | β | Causative | β-chain variant | NG_000007.3 | 71969 |
1254 | CD 131 CAG>CCG | Hb Shanghai | HBB:c.395A>C | β | Causative | β-chain variant | NG_000007.3 | 71969 |
1255 | CD 131 CAG>CAC | Hb Silver Springs | HBB:c.396G>C | β | Causative | β-chain variant | NG_000007.3 | 71970 |
1256 | CD 132 AAA>GAA [Lys>Glu] | Hb Takasago | HBB:c.397A>G | β | Causative | β-chain variant | NG_000007.3 | 71971 |
1258 | CD 132 AAA>ACA | Hb Cook | HBB:c.398A>C | β | Causative | β-chain variant | NG_000007.3 | 71972 |
1259 | CD 132 AAA>AAC, also AAA>AAT | Hb Yamagata | HBB:c.399A>C | HBB:c.399A>T | β | Causative | β-chain variant | NG_000007.3 | 71973 |
1260 | CD 133 GTG>CTG | Hb Extremadura | HBB:c.400G>C | β | Causative | β-chain variant | NG_000007.3 | 71974 |
1261 | CD 133 GTG>ATG [Val>Met] | Hb La Pommeraie | HBB:c.400G>A | β | Causative | β-chain variant | NG_000007.3 | 71974 |
3375 | CD 133 GTG>TTG [Val>Leu] | Hb Miringa | HBB:c.400G>T | β | Causative | β-chain variant | NG_000007.3 | 71974 |
1262 | CD 133 GTG>GCG | Hb Renert | HBB:c.401T>C | β | Causative | β-chain variant | NG_000007.3 | 71975 |
1263 | CD 134 GTG>GCG | Hb Yaounde | HBB:c.404T>C | β | Causative | β-chain variant | NG_000007.3 | 71978 |
2389 | CD 134 GTG>GGG [Val>Gly] | Hb Olupona | HBB:c.404T>G | β | Causative | β-chain variant | NG_000007.3 | 71978 |
1265 | CD 135 GCT>CCT [Ala>Pro] | Hb Altdorf | HBB:c.406G>C | β | Causative | β-chain variant | NG_000007.3 | 71980 |
2537 | CD 135 GCT>ACT [Ala>Thr] | Hb Calvino | HBB:c.406G>A | β | Causative | β-chain variant | NG_000007.3 | 71980 |
1266 | CD 135 GCT>GAT [Ala>Asp] | Hb Beckman | HBB:c.407C>A | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71981 |
1267 | CD 135 GCT>GTT [Ala>Val] | Hb Alperton | HBB:c.407C>T | β | Causative | β-chain variant | NG_000007.3 | 71981 |
3249 | CD 135 GCT>GC- | Hb Urumqi | HBB:c.408delT | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71982 |
1268 | CD 136 GGT>TGT [Gly>Cys] | Hb Visayan | HBB:c.409G>T | β | Causative | β-chain variant | NG_000007.3 | 71983 |
1269 | CD 136 GGT>AGT [Gly>Ser] | Hb Perpignan | HBB:c.409G>A | β | Causative | β-chain variant | NG_000007.3 | 71983 |
1270 | CD 136 GGT>CGT | Hb 'tlangeland | HBB:c.409G>C | β | Causative | β-chain variant | NG_000007.3 | 71983 |
1271 | CD 136 GGT>GCT [Gly>Ala] | Hb Petit Bourg | HBB:c.410G>C | β | Causative | β-chain variant | NG_000007.3 | 71984 |
1272 | CD 136 GGT>GAT | Hb Hope | HBB:c.410G>A | β | Causative | β-chain variant | NG_000007.3 | 71984 |
3847 | CD 136 GGT>GTT [Gly>Val] | Hb Bourg-en-Bresse | HBB:c.410G>T | β | Causative | β-chain variant | NG_000007.3 | 71984 |
3034 | CD 137 GTG>TGG [Val>Trp] | Hb Allentown | HBB:c.412_413delinsTG | β | Causative | β-chain variant | NG_000007.3 | 71986 |
1274 | CD 138 GCT>CCT [Ala>Pro] | Hb Brockton | HBB:c.415G>C | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71989 |
1275 | CD 138 GCT>ACT | Hb Buzen | HBB:c.415G>A | β | Causative | β-chain variant | NG_000007.3 | 71989 |
1276 | CD 138 GCT>GTT [Ala>Val] | Hb Cutlerville | HBB:c.416C>T | β | Causative | β-chain variant | NG_000007.3 | 71990 |
1277 | CD 139 AAT>TAT | Hb Aurora | HBB:c.418A>T | β | Causative | β-chain variant | NG_000007.3 | 71992 |
1278 | CD 139 AAT>GAT | Hb Geelong | HBB:c.418A>G | β | Causative | β-chain variant | NG_000007.3 | 71992 |
1279 | CD 139 AAT>TAT [Asn>Tyr]; CD 138 (-GCT) [-Ala] (Hb Nykerk) | Hb Nijkerk | HBB:c.[418A>T;415_417delGCT] | β | Causative | β-chain variant, Haemolytic anaemia | NG_000007.3 | 71992 |
2994 | CD 139 AAT>CAT [Asn>His] | Hb Bermondsey | HBB:c.418A>C | β | Causative | β-chain variant | NG_000007.3 | 71992 |
3370 | CD 140 GCC>ACC [Ala>Thr] AND CD 139 (-AAT) | Hb Templeuve | HBB:c.[421G>A;418_420delAAT] | β | Causative | β-chain variant | NG_000007.3 | 71992, 71995 |
1280 | CD 139 AAT>ACT | Hb Sagami | HBB:c.419A>C | β | Causative | β-chain variant | NG_000007.3 | 71993 |
3388 | CD 139 AAT>AGT [Asn>Ser] | Hb Emilia | HBB:c.419A>G | β | Causative | β-chain variant | NG_000007.3 | 71993 |
1281 | CD 139 AAT>AAR [Asn>Lys] | Hb Hinsdale | HBB:c.420T>R | β | Causative | β-chain variant | NG_000007.3 | 71994 |
1282 | CD 140 GCC>ACC | Hb Saint-Jacques | HBB:c.421G>A | β | Causative | β-chain variant | NG_000007.3 | 71995 |
1283 | CD 140 GCC>GAC [Ala>Asp] | Hb Himeji | HBB:c.422C>A | β | Causative | β-chain variant | NG_000007.3 | 71996 |
1284 | CD 140 GCC>GTC | Hb Puttelange | HBB:c.422C>T | β | Causative | β-chain variant | NG_000007.3 | 71996 |
1285 | CD 141 CTG>GTG; CD 144 AAG>TAG | Hb Kochi | HBB:c.[424C>G;433A>T] | β | Causative | β-chain variant | NG_000007.3 | 71998 |
1287 | CD 141 (-CTG) | Hb Coventry | HBB:c.424_426delCTG | β | Causative | β-chain variant | NG_000007.3 | 71998 |
2284 | CD 141 CTG>GGG | Hb Aurillac | HBB:c.424C>G | β | Causative | β-chain variant | NG_000007.3 | 71998 |
1288 | CD 141-144 (-TGGCCCACA) | Hb Birmingham | HBB:c.425_433delTGGCCCACA | β | Causative | β-chain variant | NG_000007.3 | 71999 |
1289 | CD 141 CTG>CGG | Hb Olmsted | HBB:c.425T>G | β | Causative | β-chain variant | NG_000007.3 | 71999 |
1291 | CD 142 GCC>ACC | Hb Inglewood | HBB:c.427G>A | β | Causative | β-chain variant | NG_000007.3 | 72001 |
1292 | CD 142 GCC>CCC | Hb Toyoake | HBB:c.427G>C | β | Causative | β-chain variant | NG_000007.3 | 72001 |
1293 | CD 142 GCC>GAC | Hb Ohio | HBB:c.428C>A | β | Causative | β-chain variant | NG_000007.3 | 72002 |
2297 | CD 142 GCC>GTC (Ala>Val) | Hb Waterland | HBB:c.428C>T | β | Causative | β-chain variant | NG_000007.3 | 72002 |
1295 | CD 143 CAC>GAC | Hb Rancho Mirage | HBB:c.430C>G | β | Causative | β-chain variant | NG_000007.3 | 72004 |
1296 | CD 143 CAC>AAC [His>Asn] | Hb Sapporo | HBB:c.430C>A | β | Causative | β-chain variant | NG_000007.3 | 72004 |
1297 | CD 143 CAC>TAC | Hb Old Dominion/Burton-upon-Trent (OD/BuT) | HBB:c.430C>T | β | Causative | β-chain variant | NG_000007.3 | 72004 |
1294 | CD 143 (-A) | Hb Saverne | HBB:c.431delA | β | Causative | β-chain variant | NG_000007.3 | 72005 |
1298 | CD 143 CAC>CTC [His>Leu] | Hb Vancleave | HBB:c.431A>T | β | Causative | β-chain variant | NG_000007.3 | 72005 |
1299 | CD 143 CAC>CGC | Hb Abruzzo | HBB:c.431A>G | β | Causative | β-chain variant | NG_000007.3 | 72005 |
1300 | CD 143 CAC>CCC | Hb Syracuse | HBB:c.431A>C | β | Causative | β-chain variant | NG_000007.3 | 72005 |
1301 | CD 143 CAC>CAA or CAG [His>Gln] | Hb Little Rock | HBB:c.432C>A | HBB:c.432C>G | β | Causative | β-chain variant | NG_000007.3 | 72006 |
1303 | CD 144 AAG>GAG | Hb Mito | HBB:c.433A>G | β | Causative | β-chain variant | NG_000007.3 | 72007 |
2364 | CD 144 AAG>TAG | Hb Cambridge-MA | HBB:c.433A>T | β | Causative | β-chain variant | NG_000007.3 | 72007 |
1302 | CD 144 (-A) | Hb Trento | HBB:c.434delA | β | Causative | β-chain variant | NG_000007.3 | 72008 |
1304 | CD 144 AAG>ATG | Hb Barbizon | HBB:c.434A>T | β | Causative | β-chain variant | NG_000007.3 | 72008 |
2961 | CD 144 AAG>ACG [Lys>Thr] | Hb San Cataldo | HBB:c.434A>C | β | Causative | β-chain variant | NG_000007.3 | 72008 |
3325 | CD 144 AAG>AGG [Lys>Arg] | Hb Heze | HBB:c.434A>G | β | Causative | β-chain variant | NG_000007.3 | 72008 |
1305 | CD 144 AAG>AAT or AAC | Hb Andrew-Minneapolis | HBB:c.435G>C | HBB:c.435G>T | β | Causative | β-chain variant | NG_000007.3 | 72009 |
1306 | CD 145 (+CT) | Hb Cranston | HBB:c.436_437insCT | β | Causative | β-chain variant | NG_000007.3 | 72010 |
1307 | CD 145 TAT>AAT | Hb Osler | HBB:c.436T>A | β | Causative | β-chain variant | NG_000007.3 | 72010 |
1308 | CD 145 TAT>CAT | Hb Bethesda | HBB:c.436T>C | β | Causative | β-chain variant | NG_000007.3 | 72010 |
1309 | CD 145 TAT>GAT | Hb Nancy | HBB:c.436T>G | β | Causative | β-chain variant | NG_000007.3 | 72010 |
1310 | CD 145 TAT>TGT | Hb Rainier | HBB:c.437A>G | β | Causative | β-chain variant | NG_000007.3 | 72011 |
1311 | CD 145 TAT>TAA | Hb McKees Rocks | HBB:c.438T>A | β | Causative | β-chain variant | NG_000007.3 | 72012 |
1312 | CD 146 CAC>GAC | Hb Hiroshima | HBB:c.439C>G | β | Causative | β-chain variant | NG_000007.3 | 72013 |
1313 | CD 146 CAC>TAC | Hb Bologna-St.Orsola | HBB:c.439C>T | β | Causative | β-chain variant | NG_000007.3 | 72013 |
3398 | CD 146 CAC>AAC [His>Asn] | Hb Pusan | HBB:c.439C>A | β | Causative | β-chain variant | NG_000007.3 | 72013 |
1314 | CD 146 CAC>CCC | Hb York | HBB:c.440A>C | β | Causative | β-chain variant | NG_000007.3 | 72014 |
1315 | CD 146 CAC>CTC | Hb Cowtown | HBB:c.440A>T | β | Causative | β-chain variant | NG_000007.3 | 72014 |
1316 | CD 146 CAC>CGC | Hb Cochin-Port Royal | HBB:c.440A>G | β | Causative | β-chain variant | NG_000007.3 | 72014 |
1319 | CD 146/147 (+AC) | Hb Tak | HBB:c.440_441dupAC | β | Causative | β-chain variant | NG_000007.3 | 72014 |
1317 | CD 146 CAC>CAG | Hb Kodaira II | HBB:c.441C>G | β | Causative | β-chain variant | NG_000007.3 | 72015 |
1318 | CD 146 CAC>CAA | Hb Kodaira | HBB:c.441C>A | β | Causative | β-chain variant | NG_000007.3 | 72015 |
1320 | CD 147 (+TA) | Hb Monplaisir | HBB:c.442_443dupTA | β | Causative | β-chain variant | NG_000007.3 | 72016 |
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IthaGenes was last updated on 2024-11-20 13:24:07