Linked Data
dbSNP Id:
rs778467861
ExAC:
1:230825786 T / A
gnomAD v2:
1-230825786-T-A
gnomAD v4:
1-230690040-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.230690040T>A , CM000663.2:g.230690040T>A | GRCh38 |
| NC_000001.10:g.230825786T>A , CM000663.1:g.230825786T>A | GRCh37 |
| NC_000001.9:g.228892409T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366669.9:c.1821T>A MANE Select | ENSP00000355629.4:p.Tyr607Ter | |
| ENST00000366668.7:c.1818T>A | ENSP00000355628.3:p.Tyr606Ter | |
| ENST00000366669.8:c.1821T>A | ENSP00000355629.4:p.Tyr607Ter | |
| ENST00000468893.6:c.*1679T>A | ENSP00000476305.1:n.*1679T>A | |
| ENST00000478710.1:n.80T>A | ||
| ENST00000490900.1:n.600T>A | ||
| ENST00000534989.1:c.1644T>A | ENSP00000440349.1:p.Tyr548Ter | |
| NM_001145036.1:c.1818T>A | NP_001138508.1:p.Tyr606Ter | |
| NM_007357.2:c.1821T>A | NP_031383.1:p.Tyr607Ter | |
| NM_007357.3:c.1821T>A MANE Select | NP_031383.1:p.Tyr607Ter | |
| NM_001145036.2:c.1818T>A | NP_001138508.1:p.Tyr606Ter |