Linked Data
dbSNP Id:
rs767551668
ExAC:
12:7945647 G / A
gnomAD v2:
12-7945647-G-A
gnomAD v3:
12-7793051-G-A
gnomAD v4:
12-7793051-G-A
COSMIC:
COSM5108691
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7793051G>A , CM000674.2:g.7793051G>A | GRCh38 |
| NC_000012.11:g.7945647G>A , CM000674.1:g.7945647G>A | GRCh37 |
| NC_000012.10:g.7836914G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229307.9:c.253G>A MANE Select | ENSP00000229307.4:p.Ala85Thr | |
| ENST00000229307.8:c.253G>A | ENSP00000229307.4:p.Ala85Thr | |
| ENST00000526286.1:c.253G>A | ENSP00000435288.1:p.Ala85Thr | |
| ENST00000526434.2:n.397G>A | ||
| ENST00000541267.5:c.181G>A | ENSP00000444434.1:p.Ala61Thr | |
| NM_001297698.1:c.253G>A | NP_001284627.1:p.Ala85Thr | |
| NM_024865.3:c.253G>A | NP_079141.2:p.Ala85Thr | |
| XM_011520850.1:c.253G>A | XP_011519152.1:p.Ala85Thr | |
| XM_011520851.1:c.181G>A | XP_011519153.1:p.Ala61Thr | |
| XM_011520852.1:c.-120G>A | XP_011519154.1:n.-120G>A | |
| NM_024865.4:c.253G>A MANE Select | NP_079141.2:p.Ala85Thr | |
| NM_001297698.2:c.253G>A | NP_001284627.1:p.Ala85Thr |