Linked Data
ClinVar Variation Id:
1440656
ClinVar RCV Id:
RCV001967721
dbSNP Id:
rs2125095117
COSMIC:
COSM6215060
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197102793T>C , CM000663.2:g.197102793T>C | GRCh38 |
| NC_000001.10:g.197071923T>C , CM000663.1:g.197071923T>C | GRCh37 |
| NC_000001.9:g.195338546T>C | NCBI36 |
| NG_015867.1:g.48902A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367408.6:n.2108-6629A>G | ||
| ENST00000367409.9:c.6458A>G MANE Select | ENSP00000356379.4:p.Tyr2153Cys | |
| ENST00000680265.1:c.6458A>G | ENSP00000505384.1:p.Tyr2153Cys | |
| ENST00000680710.1:c.6458A>G | ENSP00000506676.1:p.Tyr2153Cys | |
| ENST00000294732.11:c.4066-6629A>G | ENSP00000294732.7:n.4066-6629A>G | |
| ENST00000367408.5:c.1816-6629A>G | ENSP00000356378.1:n.1816-6629A>G | |
| ENST00000367409.8:c.6458A>G | ENSP00000356379.4:p.Tyr2153Cys | |
| ENST00000612785.1:c.562-146A>G | ENSP00000479244.1:n.562-146A>G | |
| NM_001206846.1:c.4066-6629A>G | NP_001193775.1:n.4066-6629A>G | |
| NM_018136.4:c.6458A>G | NP_060606.3:p.Tyr2153Cys | |
| NM_018136.5:c.6458A>G MANE Select | NP_060606.3:p.Tyr2153Cys | |
| NM_001206846.2:c.4066-6629A>G | NP_001193775.1:n.4066-6629A>G |