Linked Data
ClinVar Variation Id:
1064776
ClinVar RCV Id:
RCV001374921
dbSNP Id:
rs2150772043
COSMIC:
COSM3889463
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29530419C>T , CM000679.2:g.29530419C>T | GRCh38 |
| NC_000017.10:g.27857437C>T , CM000679.1:g.27857437C>T | GRCh37 |
| NC_000017.9:g.24881563C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261716.8:c.2161C>T MANE Select | ENSP00000261716.3:p.Gln721Ter | |
| ENST00000261716.7:c.2161C>T | ENSP00000261716.3:p.Gln721Ter | |
| ENST00000536202.1:c.1717C>T | ENSP00000438819.1:p.Gln573Ter | |
| ENST00000578653.1:n.245C>T | ||
| NM_020791.2:c.2161C>T | NP_065842.1:p.Gln721Ter | |
| NM_025142.1:c.1717C>T | NP_079418.1:p.Gln573Ter | |
| XM_011525060.1:c.2161C>T | XP_011523362.1:p.Gln721Ter | |
| XM_011525060.2:c.2161C>T | XP_011523362.1:p.Gln721Ter | |
| NM_020791.4:c.2161C>T MANE Select | NP_065842.1:p.Gln721Ter |