Linked Data
ClinVar Variation Id:
411234
dbSNP Id:
rs751362258
ExAC:
9:135772716 C / T
gnomAD v2:
9-135772716-C-T
gnomAD v3:
9-132897329-C-T
gnomAD v4:
9-132897329-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132897329C>T , CM000671.2:g.132897329C>T | GRCh38 |
| NC_000009.11:g.135772716C>T , CM000671.1:g.135772716C>T | GRCh37 |
| NC_000009.10:g.134762537C>T | NCBI36 |
| NG_012386.1:g.52305G>A , LRG_486:g.52305G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.2827G>A | ENSP00000496126.2:p.Ala943Thr | |
| ENST00000490179.4:c.2830G>A | ENSP00000495533.2:p.Ala944Thr | |
| ENST00000642261.2:c.*686G>A | ENSP00000494743.2:n.*686G>A | |
| ENST00000643275.2:c.*770G>A | ENSP00000495598.2:n.*770G>A | |
| ENST00000643362.2:c.2443G>A | ENSP00000496398.2:p.Ala815Thr | |
| ENST00000643625.2:c.*572G>A | ENSP00000495546.2:n.*572G>A | |
| ENST00000643691.2:c.2467G>A | ENSP00000494916.2:p.Ala823Thr | |
| ENST00000644184.2:c.2788G>A | ENSP00000495428.2:p.Ala930Thr | |
| ENST00000645129.2:c.2674G>A | ENSP00000493639.2:p.Ala892Thr | |
| ENST00000646440.2:c.2830G>A | ENSP00000495830.2:p.Ala944Thr | |
| ENST00000298552.9:c.2830G>A MANE Select | ENSP00000298552.3:p.Ala944Thr | |
| ENST00000642261.1:c.967G>A | ||
| ENST00000642617.1:c.2827G>A | ENSP00000493773.1:p.Ala943Thr | |
| ENST00000642627.1:c.2812G>A | ENSP00000496772.1:p.Ala938Thr | |
| ENST00000642811.1:c.*2600G>A | ENSP00000495554.1:n.*2600G>A | |
| ENST00000643072.1:c.2677G>A | ENSP00000496691.1:p.Ala893Thr | |
| ENST00000643275.1:c.1304G>A | ENSP00000495598.1:n.1304G>A | |
| ENST00000643583.1:c.2815G>A | ENSP00000494685.1:p.Ala939Thr | |
| ENST00000643625.1:c.707G>A | ENSP00000495546.1:n.707G>A | |
| ENST00000643875.1:c.2830G>A | ENSP00000495158.1:p.Ala944Thr | |
| ENST00000644097.1:c.2827G>A | ENSP00000494682.1:p.Ala943Thr | |
| ENST00000644184.1:c.1525G>A | ENSP00000495428.1:p.Ala509Thr | |
| ENST00000644255.1:c.*2597G>A | ENSP00000493608.1:n.*2597G>A | |
| ENST00000644319.1:n.3205G>A | ||
| ENST00000644786.1:n.489G>A | ||
| ENST00000644882.1:n.1738G>A | ||
| ENST00000645901.1:n.3681G>A | ||
| ENST00000646391.1:c.*2600G>A | ENSP00000494104.1:n.*2600G>A | |
| ENST00000646625.1:c.2830G>A | ENSP00000496263.1:p.Ala944Thr | |
| ENST00000647262.1:n.1795G>A | ||
| ENST00000647279.1:c.*2069G>A | ENSP00000494502.1:n.*2069G>A | |
| ENST00000647534.1:n.1894G>A | ||
| ENST00000298552.7:c.2830G>A | ENSP00000298552.3:p.Ala944Thr | |
| ENST00000440111.6:c.2830G>A | ENSP00000394524.2:p.Ala944Thr | |
| ENST00000545250.5:c.2677G>A | ENSP00000444017.1:p.Ala893Thr | |
| NM_000368.4:c.2830G>A , LRG_486t1:c.2830G>A | NP_000359.1:p.Ala944Thr | |
| NM_001162426.1:c.2827G>A | NP_001155898.1:p.Ala943Thr | |
| NM_001162427.1:c.2677G>A | NP_001155899.1:p.Ala893Thr | |
| XM_005272211.1:c.2830G>A | XP_005272268.1:p.Ala944Thr | |
| XM_006717271.1:c.2830G>A | XP_006717334.1:p.Ala944Thr | |
| XM_011518979.1:c.2830G>A | XP_011517281.1:p.Ala944Thr | |
| NM_001362177.1:c.2467G>A | NP_001349106.1:p.Ala823Thr | |
| XM_011518979.2:c.2830G>A | XP_011517281.1:p.Ala944Thr | |
| XM_017015096.1:c.2830G>A | XP_016870585.1:p.Ala944Thr | |
| XM_017015097.1:c.2830G>A | XP_016870586.1:p.Ala944Thr | |
| XM_017015098.1:c.2827G>A | XP_016870587.1:p.Ala943Thr | |
| XM_017015100.1:c.2467G>A | XP_016870589.1:p.Ala823Thr | |
| XM_017015101.1:c.2464G>A | XP_016870590.1:p.Ala822Thr | |
| NM_000368.5:c.2830G>A MANE Select | NP_000359.1:p.Ala944Thr | |
| NM_001162426.2:c.2827G>A | NP_001155898.1:p.Ala943Thr | |
| NM_001162427.2:c.2677G>A | NP_001155899.1:p.Ala893Thr | |
| NM_001362177.2:c.2467G>A | NP_001349106.1:p.Ala823Thr |