Linked Data
ClinVar Variation Id:
406674
ClinVar RCV Id:
RCV000470902
dbSNP Id:
rs121964877
COSMIC:
COSM4879157
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68822081C>G , CM000678.2:g.68822081C>G | GRCh38 |
| NC_000016.9:g.68855984C>G , CM000678.1:g.68855984C>G | GRCh37 |
| NC_000016.8:g.67413485C>G | NCBI36 |
| NG_008021.1:g.89790C>G , LRG_301:g.89790C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261769.10:c.1792C>G MANE Select | ENSP00000261769.4:p.Arg598Gly | |
| ENST00000261769.9:c.1792C>G | ENSP00000261769.4:p.Arg598Gly | |
| ENST00000422392.6:c.1609C>G | ENSP00000414946.2:p.Arg537Gly | |
| ENST00000562836.5:n.1863C>G | ||
| ENST00000566510.5:c.*458C>G | ENSP00000458139.1:n.*458C>G | |
| ENST00000566612.5:c.*32C>G | ENSP00000454782.1:n.*32C>G | |
| ENST00000611625.4:c.1855C>G | ENSP00000481063.1:p.Arg619Gly | |
| ENST00000612417.4:c.1792C>G | ENSP00000478360.1:p.Arg598Gly | |
| ENST00000621016.4:c.1792C>G | ENSP00000480664.1:p.Arg598Gly | |
| NM_004360.3:c.1792C>G , LRG_301t1:c.1792C>G | NP_004351.1:p.Arg598Gly | |
| XM_011523488.1:c.1057C>G | XP_011521790.1:p.Arg353Gly | |
| XM_011523489.1:c.1057C>G | XP_011521791.1:p.Arg353Gly | |
| NM_001317184.1:c.1609C>G | NP_001304113.1:p.Arg537Gly | |
| NM_001317185.1:c.244C>G | NP_001304114.1:p.Arg82Gly | |
| NM_001317186.1:c.-174C>G | NP_001304115.1:n.-174C>G | |
| NM_004360.4:c.1792C>G | NP_004351.1:p.Arg598Gly | |
| NM_004360.5:c.1792C>G MANE Select | NP_004351.1:p.Arg598Gly | |
| NM_001317184.2:c.1609C>G | NP_001304113.1:p.Arg537Gly | |
| NM_001317185.2:c.244C>G | NP_001304114.1:p.Arg82Gly | |
| NM_001317186.2:c.-174C>G | NP_001304115.1:n.-174C>G |