Linked Data
dbSNP Id:
rs980036132
gnomAD v3:
4-99318148-C-T
gnomAD v4:
4-99318148-C-T
COSMIC:
COSM5902680
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99318148C>T , CM000666.2:g.99318148C>T | GRCh38 |
| NC_000004.11:g.100239305C>T , CM000666.1:g.100239305C>T | GRCh37 |
| NC_000004.10:g.100458328C>T | NCBI36 |
| NG_011435.1:g.8268G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305046.13:c.157G>A MANE Select | ENSP00000306606.8:p.Val53Met | |
| ENST00000639454.1:c.157G>A | ENSP00000491622.1:p.Val53Met | |
| ENST00000305046.12:c.157G>A | ENSP00000306606.8:p.Val53Met | |
| ENST00000504498.1:n.211G>A | ||
| ENST00000506651.5:c.37G>A | ENSP00000425998.2:p.Val13Met | |
| ENST00000515694.4:n.2252G>A | ||
| ENST00000625860.2:c.37G>A | ENSP00000486614.1:p.Val13Met | |
| ENST00000632775.1:n.720G>A | ||
| NM_000668.5:c.157G>A | NP_000659.2:p.Val53Met | |
| NM_001286650.1:c.37G>A | NP_001273579.1:p.Val13Met | |
| NM_000668.6:c.157G>A MANE Select | NP_000659.2:p.Val53Met | |
| NM_001286650.2:c.37G>A | NP_001273579.1:p.Val13Met |