Linked Data
ClinVar Variation Id:
2863524
ClinVar RCV Id:
RCV003752503
dbSNP Id:
rs139816673
ExAC:
8:65517390 C / T
gnomAD v2:
8-65517390-C-T
gnomAD v4:
8-64604833-C-T
COSMIC:
COSM1101005
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64604833C>T , CM000670.2:g.64604833C>T | GRCh38 |
| NC_000008.10:g.65517390C>T , CM000670.1:g.65517390C>T | GRCh37 |
| NC_000008.9:g.65679944C>T | NCBI36 |
| NG_008338.1:g.198959G>A | |
| NG_008338.2:g.198959G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.1082G>A MANE Select | ENSP00000310721.3:p.Arg361Gln | |
| ENST00000310193.3:c.1082G>A | ENSP00000310721.3:p.Arg361Gln | |
| ENST00000523954.1:n.356G>A | ||
| NM_004820.3:c.1082G>A | NP_004811.1:p.Arg361Gln | |
| NM_001324112.1:c.1082G>A | NP_001311041.1:p.Arg361Gln | |
| NM_004820.4:c.1082G>A | NP_004811.1:p.Arg361Gln | |
| XM_017014002.1:c.1148G>A | XP_016869491.1:p.Arg383Gln | |
| NM_004820.5:c.1082G>A MANE Select | NP_004811.1:p.Arg361Gln | |
| NM_001324112.2:c.1082G>A | NP_001311041.1:p.Arg361Gln |