Linked Data
ClinVar Variation Id:
523615
ClinVar RCV Id:
RCV000627040
dbSNP Id:
rs1553698619
COSMIC:
COSM387336
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.58110018A>G , CM000665.2:g.58110018A>G | GRCh38 |
| NC_000003.11:g.58095745A>G , CM000665.1:g.58095745A>G | GRCh37 |
| NC_000003.10:g.58070785A>G | NCBI36 |
| NG_012801.1:g.106619A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682868.1:n.2475A>G | ||
| ENST00000682871.1:c.2332A>G | ENSP00000507805.1:p.Ser778Gly | |
| ENST00000684107.1:c.*864A>G | ENSP00000507440.1:n.*864A>G | |
| ENST00000684506.1:c.*864A>G | ENSP00000507728.1:n.*864A>G | |
| ENST00000684517.1:c.*864A>G | ENSP00000507828.1:n.*864A>G | |
| ENST00000684607.1:c.2332A>G | ENSP00000508224.1:p.Ser778Gly | |
| ENST00000295956.9:c.2332A>G MANE Select | ENSP00000295956.5:p.Ser778Gly | |
| ENST00000295956.8:c.2332A>G | ENSP00000295956.4:p.Ser778Gly | |
| ENST00000358537.7:c.2332A>G | ENSP00000351339.3:p.Ser778Gly | |
| ENST00000429972.6:c.2332A>G | ENSP00000415599.2:p.Ser778Gly | |
| ENST00000490882.5:c.2332A>G | ENSP00000420213.1:p.Ser778Gly | |
| ENST00000493452.5:c.1825A>G | ENSP00000418510.1:p.Ser609Gly | |
| NM_001164317.1:c.2332A>G | NP_001157789.1:p.Ser778Gly | |
| NM_001164318.1:c.2332A>G | NP_001157790.1:p.Ser778Gly | |
| NM_001164319.1:c.2332A>G | NP_001157791.1:p.Ser778Gly | |
| NM_001457.3:c.2332A>G | NP_001448.2:p.Ser778Gly | |
| XM_005264977.1:c.2332A>G | XP_005265034.1:p.Ser778Gly | |
| XM_005264978.1:c.2332A>G | XP_005265035.1:p.Ser778Gly | |
| XM_005264981.1:c.2332A>G | XP_005265038.1:p.Ser778Gly | |
| XR_940396.1:n.2477A>G | ||
| XM_005264978.2:c.2332A>G | XP_005265035.1:p.Ser778Gly | |
| XR_001740065.1:n.2477A>G | ||
| XR_940396.2:n.2477A>G | ||
| NM_001164317.2:c.2332A>G | NP_001157789.1:p.Ser778Gly | |
| NM_001164318.2:c.2332A>G | NP_001157790.1:p.Ser778Gly | |
| NM_001164319.2:c.2332A>G | NP_001157791.1:p.Ser778Gly | |
| NM_001457.4:c.2332A>G MANE Select | NP_001448.2:p.Ser778Gly |