Linked Data
ClinVar Variation Id:
2121980
ClinVar RCV Id:
RCV003053822
dbSNP Id:
rs779992896
gnomAD v4:
7-24699233-T-C
COSMIC:
COSM485225
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24699233T>C , CM000669.2:g.24699233T>C | GRCh38 |
| NC_000007.13:g.24738852T>C , CM000669.1:g.24738852T>C | GRCh37 |
| NC_000007.12:g.24705377T>C | NCBI36 |
| NG_011593.1:g.63788A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342947.9:c.1284A>G | ENSP00000339587.3:p.Val428= | |
| ENST00000409970.6:c.792A>G | ENSP00000387119.1:p.Val264= | |
| ENST00000419307.6:c.792A>G | ENSP00000401332.1:p.Val264= | |
| ENST00000645220.1:c.1284A>G MANE Select | ENSP00000494186.1:p.Val428= | |
| ENST00000342947.7:c.1284A>G | ENSP00000339587.3:p.Val428= | |
| ENST00000409775.7:c.1284A>G | ENSP00000386670.3:p.Val428= | |
| ENST00000409970.5:c.792A>G | ENSP00000387119.1:p.Val264= | |
| ENST00000419307.5:c.792A>G | ENSP00000401332.1:p.Val264= | |
| ENST00000479636.1:n.3305A>G | ||
| NM_001127453.1:c.1284A>G | NP_001120925.1:p.Val428= | |
| NM_001127454.1:c.792A>G | NP_001120926.1:p.Val264= | |
| NM_004403.2:c.1284A>G | NP_004394.1:p.Val428= | |
| XM_017011802.1:c.792A>G | XP_016867291.1:p.Val264= | |
| XM_024446670.1:c.1284A>G | XP_024302438.1:p.Val428= | |
| NM_004403.3:c.1284A>G | NP_004394.1:p.Val428= | |
| NM_001127453.2:c.1284A>G MANE Select | NP_001120925.1:p.Val428= | |
| NM_001127454.2:c.792A>G | NP_001120926.1:p.Val264= |