Linked Data
dbSNP Id:
rs72551372
ExAC:
3:119530472 G / A
gnomAD v2:
3-119530472-G-A
gnomAD v3:
3-119811625-G-A
gnomAD v4:
3-119811625-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119811625G>A , CM000665.2:g.119811625G>A | GRCh38 |
| NC_000003.11:g.119530472G>A , CM000665.1:g.119530472G>A | GRCh37 |
| NC_000003.10:g.121013162G>A | NCBI36 |
| NG_011856.1:g.36142G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000393716.8:c.418G>A MANE Select | ENSP00000377319.3:p.Val140Met | |
| ENST00000466380.6:c.418G>A | ENSP00000420297.2:p.Val140Met | |
| ENST00000337940.4:c.535G>A | ENSP00000336528.4:p.Val179Met | |
| ENST00000393716.6:c.418G>A | ENSP00000377319.2:p.Val140Met | |
| ENST00000466380.5:c.418G>A | ENSP00000420297.1:p.Val140Met | |
| ENST00000493757.1:n.550G>A | ||
| NM_003889.3:c.418G>A | NP_003880.3:p.Val140Met | |
| NM_022002.2:c.535G>A | NP_071285.1:p.Val179Met | |
| NM_033013.2:c.418G>A | NP_148934.1:p.Val140Met | |
| NM_003889.4:c.418G>A MANE Select | NP_003880.3:p.Val140Met | |
| NM_022002.3:c.535G>A | NP_071285.1:p.Val179Met | |
| NM_033013.3:c.418G>A | NP_148934.1:p.Val140Met |