Linked Data
dbSNP Id:
rs775156579
ExAC:
1:9017322 A / T
gnomAD v2:
1-9017322-A-T
gnomAD v4:
1-8957263-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.8957263A>T , CM000663.2:g.8957263A>T | GRCh38 |
| NC_000001.10:g.9017322A>T , CM000663.1:g.9017322A>T | GRCh37 |
| NC_000001.9:g.8939909A>T | NCBI36 |
| NG_033975.1:g.16430A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377443.7:c.386A>T MANE Select | ENSP00000366662.2:p.Asp129Val | |
| ENST00000377436.6:c.386A>T | ENSP00000366654.3:p.Asp129Val | |
| ENST00000377442.3:c.206A>T | ENSP00000366661.2:p.Asp69Val | |
| ENST00000377443.6:c.386A>T | ENSP00000366662.2:p.Asp129Val | |
| ENST00000476083.1:n.99-1647A>T | ||
| ENST00000549778.5:c.290A>T | ENSP00000447108.1:p.Asp97Val | |
| NM_001215.3:c.386A>T | NP_001206.2:p.Asp129Val | |
| NM_001270500.1:c.386A>T | NP_001257429.1:p.Asp129Val | |
| NM_001270501.1:c.206A>T | NP_001257430.1:p.Asp69Val | |
| NM_001270502.1:c.25-1647A>T | NP_001257431.1:n.25-1647A>T | |
| XM_011542083.1:c.398A>T | XP_011540385.1:p.Asp133Val | |
| XM_011542084.1:c.398A>T | XP_011540386.1:p.Asp133Val | |
| XM_011542083.3:c.398A>T | XP_011540385.1:p.Asp133Val | |
| XM_011542084.3:c.398A>T | XP_011540386.1:p.Asp133Val | |
| NM_001215.4:c.386A>T MANE Select | NP_001206.2:p.Asp129Val | |
| NM_001270500.2:c.386A>T | NP_001257429.1:p.Asp129Val | |
| NM_001270501.2:c.206A>T | NP_001257430.1:p.Asp69Val | |
| NM_001270502.2:c.25-1647A>T | NP_001257431.1:n.25-1647A>T |