Linked Data
ClinVar Variation Id:
92371
dbSNP Id:
rs376371866
gnomAD v3:
9-130476878-C-A
gnomAD v4:
9-130476878-C-A
PubMed:
PMID:23891399
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130476878C>A , CM000671.2:g.130476878C>A | GRCh38 |
| NC_000009.11:g.133352265C>A , CM000671.1:g.133352265C>A | GRCh37 |
| NC_000009.10:g.132342086C>A | NCBI36 |
| NG_011542.1:g.37172C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352480.10:c.605C>A MANE Select | ENSP00000253004.6:p.Ala202Glu | |
| ENST00000352480.9:c.605C>A | ENSP00000253004.6:p.Ala202Glu | |
| ENST00000372393.7:c.605C>A | ENSP00000361469.2:p.Ala202Glu | |
| ENST00000372394.5:c.605C>A | ENSP00000361471.1:p.Ala202Glu | |
| ENST00000467695.5:n.314C>A | ||
| ENST00000470849.4:n.330C>A | ||
| ENST00000492400.5:n.114C>A | ||
| ENST00000493984.6:n.436C>A | ||
| NM_000050.4:c.605C>A | NP_000041.2:p.Ala202Glu | |
| NM_054012.3:c.605C>A | NP_446464.1:p.Ala202Glu | |
| XM_005272200.2:c.605C>A | XP_005272257.1:p.Ala202Glu | |
| XM_011518705.1:c.719C>A | XP_011517007.1:p.Ala240Glu | |
| XM_005272200.3:c.605C>A | XP_005272257.1:p.Ala202Glu | |
| XM_011518705.2:c.719C>A | XP_011517007.1:p.Ala240Glu | |
| XM_017014729.1:c.701C>A | XP_016870218.1:p.Ala234Glu | |
| NM_054012.4:c.605C>A MANE Select | NP_446464.1:p.Ala202Glu |