Linked Data
ClinVar Variation Id:
1759932
ClinVar RCV Id:
RCV002396350
dbSNP Id:
rs111372278
gnomAD v2:
1-15772215-G-A
gnomAD v4:
1-15445720-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445720G>A , CM000663.2:g.15445720G>A | GRCh38 |
| NC_000001.10:g.15772215G>A , CM000663.1:g.15772215G>A | GRCh37 |
| NC_000001.9:g.15644802G>A | NCBI36 |
| NG_009253.1:g.12278G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.763G>A MANE Select | ENSP00000365116.4:p.Val255Met | |
| ENST00000375943.6:c.*217G>A | ENSP00000365110.2:n.*217G>A | |
| ENST00000375949.4:c.763G>A | ENSP00000365116.4:p.Val255Met | |
| ENST00000483406.1:n.527G>A | ||
| NM_007272.2:c.763G>A | NP_009203.2:p.Val255Met | |
| XM_011540550.1:c.617G>A | XP_011538852.1:p.Gly206Asp | |
| NM_007272.3:c.763G>A MANE Select | NP_009203.2:p.Val255Met |