Linked Data
ClinVar Variation Id:
418854
dbSNP Id:
rs749727182
gnomAD v2:
7-6026631-C-G
gnomAD v3:
7-5987000-C-G
gnomAD v4:
7-5987000-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5987000C>G , CM000669.2:g.5987000C>G | GRCh38 |
| NC_000007.13:g.6026631C>G , CM000669.1:g.6026631C>G | GRCh37 |
| NC_000007.12:g.5993157C>G | NCBI36 |
| NG_008466.1:g.27107G>C , LRG_161:g.27107G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*1161G>C | ENSP00000514615.2:n.*1161G>C | |
| ENST00000699840.2:c.1762G>C | ENSP00000514638.2:p.Asp588His | |
| ENST00000699930.2:c.1657G>C | ENSP00000514695.2:p.Asp553His | |
| ENST00000406569.8:c.1678+87G>C | ENSP00000514464.1:n.1678+87G>C | |
| ENST00000644110.2:c.*1359G>C | ENSP00000496392.2:n.*1359G>C | |
| ENST00000699752.1:c.1609G>C | ENSP00000514561.1:p.Asp537His | |
| ENST00000699753.1:c.*1186G>C | ENSP00000514562.1:n.*1186G>C | |
| ENST00000699754.1:c.1567G>C | ENSP00000514563.1:p.Asp523His | |
| ENST00000699755.1:c.*1164G>C | ENSP00000514564.1:n.*1164G>C | |
| ENST00000699756.1:c.*1352G>C | ENSP00000514565.1:n.*1352G>C | |
| ENST00000699757.1:c.*1022G>C | ENSP00000514566.1:n.*1022G>C | |
| ENST00000699758.1:c.*1022G>C | ENSP00000514567.1:n.*1022G>C | |
| ENST00000699759.1:n.2619G>C | ||
| ENST00000699760.1:c.1447G>C | ENSP00000514568.1:p.Asp483His | |
| ENST00000699761.1:c.1360G>C | ENSP00000514569.1:p.Asp454His | |
| ENST00000699762.1:c.1192G>C | ENSP00000514570.1:p.Asp398His | |
| ENST00000699763.1:c.*855G>C | ENSP00000514571.1:n.*855G>C | |
| ENST00000699764.1:c.*83G>C | ENSP00000514572.1:n.*83G>C | |
| ENST00000699765.1:c.*861G>C | ENSP00000514573.1:n.*861G>C | |
| ENST00000699766.1:c.1765G>C | ENSP00000514574.1:p.Asp589His | |
| ENST00000699767.1:c.1765G>C | ENSP00000514575.1:p.Asp589His | |
| ENST00000699768.1:c.1765G>C | ENSP00000514576.1:p.Asp589His | |
| ENST00000699811.1:c.1360G>C | ENSP00000514614.1:p.Asp454His | |
| ENST00000699813.1:n.1878G>C | ||
| ENST00000699814.1:c.1388G>C | ||
| ENST00000699815.1:c.*1296G>C | ENSP00000514616.1:n.*1296G>C | |
| ENST00000699816.1:c.*655G>C | ENSP00000514617.1:n.*655G>C | |
| ENST00000699817.1:c.*1359G>C | ENSP00000514618.1:n.*1359G>C | |
| ENST00000699818.1:c.1360G>C | ENSP00000514619.1:p.Asp454His | |
| ENST00000699819.1:c.*922G>C | ENSP00000514620.1:n.*922G>C | |
| ENST00000699820.1:c.1144+2800G>C | ENSP00000514621.1:n.1144+2800G>C | |
| ENST00000699821.1:c.1360G>C | ENSP00000514622.1:p.Asp454His | |
| ENST00000699822.1:c.*1217G>C | ENSP00000514623.1:n.*1217G>C | |
| ENST00000699823.1:c.1360G>C | ENSP00000514624.1:p.Asp454His | |
| ENST00000699824.1:c.*1268G>C | ENSP00000514625.1:n.*1268G>C | |
| ENST00000699825.1:c.1204G>C | ENSP00000514626.1:p.Asp402His | |
| ENST00000699826.1:c.*1164G>C | ENSP00000514627.1:n.*1164G>C | |
| ENST00000699827.1:c.1597G>C | ENSP00000514628.1:p.Asp533His | |
| ENST00000699828.1:c.*855G>C | ENSP00000514629.1:n.*855G>C | |
| ENST00000699833.1:n.3537G>C | ||
| ENST00000699837.1:c.1360G>C | ENSP00000514635.1:p.Asp454His | |
| ENST00000699838.1:c.*1665G>C | ENSP00000514636.1:n.*1665G>C | |
| ENST00000699839.1:c.1951G>C | ENSP00000514637.1:p.Asp651His | |
| ENST00000699916.1:c.*1022G>C | ENSP00000514684.1:n.*1022G>C | |
| ENST00000699917.1:c.*1214G>C | ENSP00000514685.1:n.*1214G>C | |
| ENST00000699918.1:c.*1266G>C | ENSP00000514686.1:n.*1266G>C | |
| ENST00000699919.1:c.*1352G>C | ENSP00000514687.1:n.*1352G>C | |
| ENST00000699920.1:c.*1401G>C | ENSP00000514688.1:n.*1401G>C | |
| ENST00000699928.1:c.989-4009G>C | ENSP00000514693.1:n.989-4009G>C | |
| ENST00000699929.1:c.*1066G>C | ENSP00000514694.1:n.*1066G>C | |
| ENST00000699930.1:c.1657G>C | ENSP00000514695.1:p.Asp553His | |
| ENST00000699931.1:n.3193G>C | ||
| ENST00000699951.1:c.*861G>C | ENSP00000514706.1:n.*861G>C | |
| ENST00000699952.1:c.803+10326G>C | ENSP00000514707.1:n.803+10326G>C | |
| ENST00000699953.1:c.*872G>C | ENSP00000514708.1:n.*872G>C | |
| ENST00000699954.1:c.*1066G>C | ENSP00000514709.1:n.*1066G>C | |
| ENST00000265849.12:c.1765G>C MANE Select | ENSP00000265849.7:p.Asp589His | |
| ENST00000642292.1:c.1360G>C | ENSP00000495524.1:p.Asp454His | |
| ENST00000642456.1:c.1360G>C | ENSP00000493814.1:p.Asp454His | |
| ENST00000643595.1:c.*1164G>C | ENSP00000494497.1:n.*1164G>C | |
| ENST00000644110.1:c.1447G>C | ENSP00000496392.1:p.Asp483His | |
| ENST00000265849.11:c.1765G>C | ENSP00000265849.7:p.Asp589His | |
| ENST00000382321.5:c.804-4009G>C | ENSP00000371758.4:n.804-4009G>C | |
| ENST00000406569.7:n.1678+87G>C | ||
| ENST00000441476.6:c.1447G>C | ENSP00000392843.2:p.Asp483His | |
| ENST00000469652.1:n.63-4095G>C | ||
| NM_000535.5:c.1765G>C , LRG_161t1:c.1765G>C | NP_000526.1:p.Asp589His | |
| NR_003085.2:n.1847G>C | ||
| XM_006715742.2:c.1759G>C | XP_006715805.1:p.Asp587His | |
| XM_006715744.2:c.832G>C | XP_006715807.1:p.Asp278His | |
| XM_011515427.1:c.1810G>C | XP_011513729.1:p.Asp604His | |
| XM_011515428.1:c.1654G>C | XP_011513730.1:p.Asp552His | |
| XM_011515429.1:c.1447G>C | XP_011513731.1:p.Asp483His | |
| XM_011515430.1:c.1447G>C | XP_011513732.1:p.Asp483His | |
| NM_000535.6:c.1765G>C | NP_000526.2:p.Asp589His | |
| NM_001322003.1:c.1360G>C | NP_001308932.1:p.Asp454His | |
| NM_001322004.1:c.1360G>C | NP_001308933.1:p.Asp454His | |
| NM_001322005.1:c.1360G>C | NP_001308934.1:p.Asp454His | |
| NM_001322006.1:c.1609G>C | NP_001308935.1:p.Asp537His | |
| NM_001322007.1:c.1447G>C | NP_001308936.1:p.Asp483His | |
| NM_001322008.1:c.1447G>C | NP_001308937.1:p.Asp483His | |
| NM_001322009.1:c.1360G>C | NP_001308938.1:p.Asp454His | |
| NM_001322010.1:c.1204G>C | NP_001308939.1:p.Asp402His | |
| NM_001322011.1:c.832G>C | NP_001308940.1:p.Asp278His | |
| NM_001322012.1:c.832G>C | NP_001308941.1:p.Asp278His | |
| NM_001322013.1:c.1192G>C | NP_001308942.1:p.Asp398His | |
| NM_001322014.1:c.1765G>C | NP_001308943.1:p.Asp589His | |
| NM_001322015.1:c.1456G>C | NP_001308944.1:p.Asp486His | |
| NR_136154.1:n.1852G>C | ||
| XM_006715744.4:c.832G>C | XP_006715807.1:p.Asp278His | |
| XM_017012342.2:c.832G>C | XP_016867831.1:p.Asp278His | |
| XM_024446800.1:c.1204G>C | XP_024302568.1:p.Asp402His | |
| NM_000535.7:c.1765G>C MANE Select | NP_000526.2:p.Asp589His | |
| NM_001322003.2:c.1360G>C | NP_001308932.1:p.Asp454His | |
| NM_001322004.2:c.1360G>C | NP_001308933.1:p.Asp454His | |
| NM_001322005.2:c.1360G>C | NP_001308934.1:p.Asp454His | |
| NM_001322006.2:c.1609G>C | NP_001308935.1:p.Asp537His | |
| NM_001322008.2:c.1447G>C | NP_001308937.1:p.Asp483His | |
| NM_001322009.2:c.1360G>C | NP_001308938.1:p.Asp454His | |
| NM_001322010.2:c.1204G>C | NP_001308939.1:p.Asp402His | |
| NM_001322011.2:c.832G>C | NP_001308940.1:p.Asp278His | |
| NM_001322012.2:c.832G>C | NP_001308941.1:p.Asp278His | |
| NM_001322013.2:c.1192G>C | NP_001308942.1:p.Asp398His | |
| NM_001322014.2:c.1765G>C | NP_001308943.1:p.Asp589His | |
| NM_001322015.2:c.1456G>C | NP_001308944.1:p.Asp486His | |
| NM_001322007.2:c.1447G>C | NP_001308936.1:p.Asp483His |