Linked Data
ClinVar Variation Id:
1775223
ClinVar RCV Id:
RCV002405376
dbSNP Id:
rs878854573
gnomAD v2:
1-17371301-G-A
gnomAD v4:
1-17044806-G-A
COSMIC:
COSM5595282
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17044806G>A , CM000663.2:g.17044806G>A | GRCh38 |
| NC_000001.10:g.17371301G>A , CM000663.1:g.17371301G>A | GRCh37 |
| NC_000001.9:g.17243888G>A | NCBI36 |
| NG_012340.1:g.14365C>T , LRG_316:g.14365C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.-17C>T | ENSP00000481376.2:n.-17C>T | |
| ENST00000491274.6:c.113C>T | ENSP00000480482.2:p.Ala38Val | |
| ENST00000375499.8:c.155C>T MANE Select | ENSP00000364649.3:p.Ala52Val | |
| ENST00000375499.7:c.155C>T | ENSP00000364649.3:p.Ala52Val | |
| ENST00000463045.2:c.-17C>T | ENSP00000481376.1:n.-17C>T | |
| ENST00000466613.2:n.167C>T | ||
| ENST00000475506.1:n.72C>T | ||
| ENST00000485515.5:n.143C>T | ||
| ENST00000491274.5:c.113C>T | ENSP00000480482.1:p.Ala38Val | |
| NM_003000.2:c.155C>T , LRG_316t1:c.155C>T | NP_002991.2:p.Ala52Val | |
| NM_003000.3:c.155C>T MANE Select | NP_002991.2:p.Ala52Val |