Linked Data
ClinVar Variation Id:
514656
dbSNP Id:
rs367790253
ExAC:
8:75276245 C / T
gnomAD v2:
8-75276245-C-T
gnomAD v3:
8-74364010-C-T
gnomAD v4:
8-74364010-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.74364010C>T , CM000670.2:g.74364010C>T | GRCh38 |
| NC_000008.10:g.75276245C>T , CM000670.1:g.75276245C>T | GRCh37 |
| NC_000008.9:g.75438800C>T | NCBI36 |
| NG_008787.2:g.47881C>T | |
| NG_008787.3:g.47881C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220822.12:c.720C>T MANE Select | ENSP00000220822.7:p.Cys240= | |
| ENST00000434412.3:c.588C>T | ENSP00000417006.3:p.Cys196= | |
| ENST00000520797.6:n.831C>T | ||
| ENST00000521096.6:n.576C>T | ||
| ENST00000522568.2:c.*392C>T | ENSP00000430136.1:n.*392C>T | |
| ENST00000523640.2:c.165+12689C>T | ENSP00000502017.1:n.165+12689C>T | |
| ENST00000524195.2:c.280+957C>T | ENSP00000502308.1:n.280+957C>T | |
| ENST00000674612.1:c.393C>T | ENSP00000501864.1:p.Cys131= | |
| ENST00000674710.1:c.694+957C>T | ENSP00000502762.1:n.694+957C>T | |
| ENST00000674754.1:c.*2283C>T | ENSP00000502063.1:n.*2283C>T | |
| ENST00000674756.1:c.*366+957C>T | ENSP00000501860.1:n.*366+957C>T | |
| ENST00000674806.1:c.393C>T | ENSP00000502637.1:p.Cys131= | |
| ENST00000674865.1:c.516C>T | ENSP00000502437.1:p.Cys172= | |
| ENST00000674926.1:c.*1352C>T | ENSP00000501799.1:n.*1352C>T | |
| ENST00000674934.1:c.*408C>T | ENSP00000502187.1:n.*408C>T | |
| ENST00000674944.1:c.*1323C>T | ENSP00000501858.1:n.*1323C>T | |
| ENST00000674946.1:c.694+957C>T | ENSP00000501569.1:n.694+957C>T | |
| ENST00000674973.1:c.414C>T | ENSP00000502447.1:p.Cys138= | |
| ENST00000675007.1:c.*458C>T | ENSP00000502119.1:n.*458C>T | |
| ENST00000675060.1:c.*385C>T | ENSP00000501616.1:n.*385C>T | |
| ENST00000675165.1:c.717C>T | ENSP00000502612.1:p.Cys239= | |
| ENST00000675220.1:c.393C>T | ENSP00000502588.1:p.Cys131= | |
| ENST00000675265.1:c.*470C>T | ENSP00000501848.1:n.*470C>T | |
| ENST00000675336.1:c.*206C>T | ENSP00000502120.1:n.*206C>T | |
| ENST00000675376.1:c.393C>T | ENSP00000502838.1:p.Cys131= | |
| ENST00000675463.1:c.798C>T | ENSP00000502327.1:p.Cys266= | |
| ENST00000675472.1:c.*206C>T | ENSP00000501946.1:n.*206C>T | |
| ENST00000675474.1:n.305C>T | ||
| ENST00000675560.1:c.*366+957C>T | ENSP00000502118.1:n.*366+957C>T | |
| ENST00000675625.1:c.*392C>T | ENSP00000501626.1:n.*392C>T | |
| ENST00000675633.1:c.*127C>T | ENSP00000501785.1:n.*127C>T | |
| ENST00000675661.1:c.*480C>T | ENSP00000501958.1:n.*480C>T | |
| ENST00000675706.1:n.2678C>T | ||
| ENST00000675821.1:c.393C>T | ENSP00000502198.1:p.Cys131= | |
| ENST00000675832.1:c.*392C>T | ENSP00000502041.1:n.*392C>T | |
| ENST00000675928.1:c.546C>T | ENSP00000501568.1:p.Cys182= | |
| ENST00000675944.1:c.516C>T | ENSP00000502673.1:p.Cys172= | |
| ENST00000675999.1:c.694+957C>T | ENSP00000502572.1:n.694+957C>T | |
| ENST00000676049.1:c.*622C>T | ENSP00000501912.1:n.*622C>T | |
| ENST00000676112.1:c.786C>T | ENSP00000502295.1:p.Cys262= | |
| ENST00000676143.1:c.393C>T | ENSP00000502828.1:p.Cys131= | |
| ENST00000676207.1:c.694+957C>T | ENSP00000502638.1:n.694+957C>T | |
| ENST00000676377.1:c.393C>T | ENSP00000502756.1:p.Cys131= | |
| ENST00000676415.1:c.*26C>T | ENSP00000502665.1:n.*26C>T | |
| ENST00000676443.1:c.672C>T | ENSP00000501769.1:p.Cys224= | |
| ENST00000220822.11:c.720C>T | ENSP00000220822.7:p.Cys240= | |
| ENST00000434412.2:c.516C>T | ENSP00000417006.2:p.Cys172= | |
| ENST00000520797.5:n.485C>T | ||
| ENST00000521096.5:n.526C>T | ||
| ENST00000522568.1:c.*392C>T | ENSP00000430136.1:n.*392C>T | |
| ENST00000524195.1:n.103+957C>T | ||
| ENST00000524366.5:n.564C>T | ||
| NM_001040875.2:c.516C>T | NP_001035808.1:p.Cys172= | |
| NM_018972.2:c.720C>T | NP_061845.2:p.Cys240= | |
| NR_046346.1:n.654C>T | ||
| XM_011517551.1:c.1014C>T | XP_011515853.1:p.Cys338= | |
| XM_011517552.1:c.393C>T | XP_011515854.1:p.Cys131= | |
| NM_001040875.3:c.516C>T | NP_001035808.1:p.Cys172= | |
| NM_001362929.1:c.393C>T | NP_001349858.1:p.Cys131= | |
| NM_001362930.1:c.546C>T | NP_001349859.1:p.Cys182= | |
| NM_001362931.1:c.694+957C>T | NP_001349860.1:n.694+957C>T | |
| NM_001362932.1:c.393C>T | NP_001349861.1:p.Cys131= | |
| NM_018972.3:c.720C>T | NP_061845.2:p.Cys240= | |
| NM_001362931.2:c.694+957C>T | NP_001349860.1:n.694+957C>T | |
| NM_018972.4:c.720C>T MANE Select | NP_061845.2:p.Cys240= | |
| NM_001040875.4:c.516C>T | NP_001035808.1:p.Cys172= | |
| NM_001362929.2:c.393C>T | NP_001349858.1:p.Cys131= | |
| NM_001362930.2:c.546C>T | NP_001349859.1:p.Cys182= | |
| NM_001362932.2:c.393C>T | NP_001349861.1:p.Cys131= |