Linked Data
dbSNP Id:
rs777725359
ExAC:
16:2328338 C / T
gnomAD v2:
16-2328338-C-T
gnomAD v3:
16-2278337-C-T
gnomAD v4:
16-2278337-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2278337C>T , CM000678.2:g.2278337C>T | GRCh38 |
| NC_000016.9:g.2328338C>T , CM000678.1:g.2328338C>T | GRCh37 |
| NC_000016.8:g.2268339C>T | NCBI36 |
| NG_011790.1:g.67410G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4669G>A MANE Select | ENSP00000301732.5:p.Val1557Met | |
| ENST00000301732.9:c.4669G>A | ENSP00000301732.5:p.Val1557Met | |
| ENST00000382381.7:c.4495G>A | ENSP00000371818.3:p.Val1499Met | |
| ENST00000566200.1:n.1190G>A | ||
| NM_001089.2:c.4669G>A | NP_001080.2:p.Val1557Met | |
| NM_001089.3:c.4669G>A MANE Select | NP_001080.2:p.Val1557Met |