Linked Data
ClinVar Variation Id:
585750
ClinVar RCV Id:
RCV000711373
dbSNP Id:
rs200005406
ExAC:
6:32008874 G / A
gnomAD v2:
6-32008874-G-A
gnomAD v3:
6-32041097-G-A
gnomAD v4:
6-32041097-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32041097G>A , CM000668.2:g.32041097G>A | GRCh38 |
| NC_000006.11:g.32008874G>A , CM000668.1:g.32008874G>A | GRCh37 |
| NC_000006.10:g.32116853G>A | NCBI36 |
| NG_007941.2:g.7790G>A | |
| NG_008337.2:g.73278C>T | |
| NG_007941.3:g.7793G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644719.2:c.1451G>A MANE Select | ENSP00000496625.1:p.Arg484Gln | |
| ENST00000418967.6:c.1451G>A | ENSP00000408860.2:p.Arg484Gln | |
| ENST00000435122.3:c.1361G>A | ENSP00000415043.2:p.Arg454Gln | |
| ENST00000479074.5:n.1592G>A | ||
| ENST00000479730.5:n.1567G>A | ||
| ENST00000483041.5:n.1620G>A | ||
| ENST00000486063.5:n.1430G>A | ||
| NM_000500.7:c.1451G>A | NP_000491.4:p.Arg484Gln | |
| NM_001128590.3:c.1361G>A | NP_001122062.3:p.Arg454Gln | |
| XM_011514314.1:c.1046G>A | XP_011512616.1:p.Arg349Gln | |
| NM_000500.9:c.1451G>A MANE Select | NP_000491.4:p.Arg484Gln | |
| NM_001368143.1:c.1046G>A | NP_001355072.1:p.Arg349Gln | |
| NM_001368144.1:c.1046G>A | NP_001355073.1:p.Arg349Gln | |
| NM_001128590.4:c.1361G>A | NP_001122062.3:p.Arg454Gln | |
| NM_001368143.2:c.1046G>A | NP_001355072.1:p.Arg349Gln | |
| NM_001368144.2:c.1046G>A | NP_001355073.1:p.Arg349Gln |