Linked Data
ClinVar Variation Id:
133289
dbSNP Id:
rs587777404
ExAC:
1:64100604 G / T
gnomAD v2:
1-64100604-G-T
gnomAD v3:
1-63634933-G-T
gnomAD v4:
1-63634933-G-T
PubMed:
PMID:24499211
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.63634933G>T , CM000663.2:g.63634933G>T | GRCh38 |
| NC_000001.10:g.64100604G>T , CM000663.1:g.64100604G>T | GRCh37 |
| NC_000001.9:g.63873192G>T | NCBI36 |
| NG_016966.1:g.46658G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371084.8:c.787G>T MANE Select | ENSP00000360125.3:p.Asp263Tyr | |
| ENST00000650546.1:c.787G>T | ENSP00000497812.1:p.Asp263Tyr | |
| ENST00000371083.4:c.841G>T | ENSP00000360124.4:p.Asp281Tyr | |
| ENST00000371084.7:c.787G>T | ENSP00000360125.3:p.Asp263Tyr | |
| ENST00000540265.5:c.196G>T | ENSP00000443449.1:p.Asp66Tyr | |
| NM_001172818.1:c.841G>T | NP_001166289.1:p.Asp281Tyr | |
| NM_001172819.1:c.196G>T | NP_001166290.1:p.Asp66Tyr | |
| NM_002633.2:c.787G>T | NP_002624.2:p.Asp263Tyr | |
| NM_002633.3:c.787G>T MANE Select | NP_002624.2:p.Asp263Tyr | |
| NM_001172819.2:c.196G>T | NP_001166290.1:p.Asp66Tyr |