Linked Data
ClinVar Variation Id:
120285
ClinVar RCV Id:
RCV000106366
dbSNP Id:
rs281865445
gnomAD v4:
12-102852872-A-C
ERepo:
CA267671/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852872A>C , CM000674.2:g.102852872A>C | GRCh38 |
| NC_000012.11:g.103246650A>C , CM000674.1:g.103246650A>C | GRCh37 |
| NC_000012.10:g.101770780A>C | NCBI36 |
| NG_008690.1:g.69731T>G | |
| NG_008690.2:g.110539T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.785T>G MANE Select | ENSP00000448059.1:p.Val262Gly | |
| ENST00000307000.7:c.770T>G | ENSP00000303500.2:p.Val257Gly | |
| ENST00000549247.6:n.544T>G | ||
| ENST00000553106.5:c.785T>G | ENSP00000448059.1:p.Val262Gly | |
| NM_000277.1:c.785T>G | NP_000268.1:p.Val262Gly | |
| XM_011538422.1:c.785T>G | XP_011536724.1:p.Val262Gly | |
| NM_000277.2:c.785T>G | NP_000268.1:p.Val262Gly | |
| NM_001354304.1:c.785T>G | NP_001341233.1:p.Val262Gly | |
| NM_000277.3:c.785T>G MANE Select | NP_000268.1:p.Val262Gly | |
| NM_001354304.2:c.785T>G | NP_001341233.1:p.Val262Gly |