Linked Data
ClinVar Variation Id:
97152
dbSNP Id:
rs66550389
COSMIC:
COSM276565
PubMed:
PMID:1671317
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38369854G>A , CM000685.2:g.38369854G>A | GRCh38 |
| NC_000023.10:g.38229107G>A , CM000685.1:g.38229107G>A | GRCh37 |
| NC_000023.9:g.38114051G>A | NCBI36 |
| NG_008471.1:g.22372G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.275G>A MANE Select | ENSP00000039007.4:p.Arg92Gln | |
| ENST00000643344.1:c.275G>A | ENSP00000496606.1:p.Arg92Gln | |
| ENST00000039007.4:c.275G>A | ENSP00000039007.4:p.Arg92Gln | |
| ENST00000465127.1:c.172-296267G>A | ENSP00000417050.1:n.172-296267G>A | |
| ENST00000488812.1:n.353+14G>A | ||
| NM_000531.5:c.275G>A | NP_000522.3:p.Arg92Gln | |
| XM_017029556.1:c.275G>A | XP_016885045.1:p.Arg92Gln | |
| NM_000531.6:c.275G>A MANE Select | NP_000522.3:p.Arg92Gln |