Linked Data
ClinVar Variation Id:
208267
ClinVar RCV Id:
RCV000206955
dbSNP Id:
rs864621984
gnomAD v4:
19-12657507-G-T
PubMed:
PMID:22161967
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12657507G>T , CM000681.2:g.12657507G>T | GRCh38 |
| NC_000019.9:g.12768321G>T , CM000681.1:g.12768321G>T | GRCh37 |
| NC_000019.8:g.12629321G>T | NCBI36 |
| NG_008318.1:g.14271C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456935.7:c.1358C>A MANE Select | ENSP00000395473.2:p.Ser453Tyr | |
| ENST00000221363.8:c.1355C>A | ENSP00000221363.4:p.Ser452Tyr | |
| ENST00000456935.6:c.1358C>A | ENSP00000395473.2:p.Ser453Tyr | |
| ENST00000465830.1:n.522C>A | ||
| ENST00000466794.5:n.1257C>A | ||
| ENST00000495617.1:n.534C>A | ||
| NM_000528.3:c.1358C>A | NP_000519.2:p.Ser453Tyr | |
| NM_001173498.1:c.1355C>A | NP_001166969.1:p.Ser452Tyr | |
| XM_005259913.1:c.1361C>A | XP_005259970.1:p.Ser454Tyr | |
| XM_011528017.1:c.257C>A | XP_011526319.1:p.Ser86Tyr | |
| XM_005259913.2:c.1361C>A | XP_005259970.1:p.Ser454Tyr | |
| XM_024451518.1:c.257C>A | XP_024307286.1:p.Ser86Tyr | |
| NM_000528.4:c.1358C>A MANE Select | NP_000519.2:p.Ser453Tyr | |
| NM_001173498.2:c.1355C>A | NP_001166969.1:p.Ser452Tyr |