Linked Data
ClinVar Variation Id:
419347
dbSNP Id:
rs200007766
ExAC:
20:61981657 C / T
gnomAD v2:
20-61981657-C-T
gnomAD v3:
20-63350305-C-T
gnomAD v4:
20-63350305-C-T
COSMIC:
COSM1201122
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63350305C>T , CM000682.2:g.63350305C>T | GRCh38 |
| NC_000020.10:g.61981657C>T , CM000682.1:g.61981657C>T | GRCh37 |
| NC_000020.9:g.61452101C>T | NCBI36 |
| NG_011931.1:g.16039G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370263.9:c.1106G>A MANE Select | ENSP00000359285.4:p.Arg369Gln | |
| ENST00000370263.8:c.1106G>A | ENSP00000359285.4:p.Arg369Gln | |
| ENST00000463705.5:n.1754G>A | ||
| ENST00000467563.3:n.1176G>A | ||
| ENST00000498043.6:c.1130G>A | ||
| ENST00000615287.4:c.893G>A | ENSP00000483388.1:p.Arg298Gln | |
| ENST00000627000.1:c.*795G>A | ENSP00000486914.1:n.*795G>A | |
| ENST00000630240.1:n.827G>A | ||
| NM_000744.6:c.1106G>A | NP_000735.1:p.Arg369Gln | |
| NM_001256573.1:c.578G>A | NP_001243502.1:p.Arg193Gln | |
| NR_046317.1:n.1362G>A | ||
| XM_011528524.1:c.893G>A | XP_011526826.1:p.Arg298Gln | |
| XM_017027625.2:c.578G>A | XP_016883114.1:p.Arg193Gln | |
| XM_024451822.1:c.578G>A | XP_024307590.1:p.Arg193Gln | |
| NM_001256573.2:c.578G>A | NP_001243502.1:p.Arg193Gln | |
| NR_046317.2:n.1315G>A | ||
| NM_000744.7:c.1106G>A MANE Select | NP_000735.1:p.Arg369Gln |