Linked Data
ClinVar Variation Id:
1363368
ClinVar RCV Id:
RCV001902220
dbSNP Id:
rs533428309
ExAC:
19:12767846 G / A
gnomAD v2:
19-12767846-G-A
gnomAD v3:
19-12657032-G-A
gnomAD v4:
19-12657032-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12657032G>A , CM000681.2:g.12657032G>A | GRCh38 |
| NC_000019.9:g.12767846G>A , CM000681.1:g.12767846G>A | GRCh37 |
| NC_000019.8:g.12628846G>A | NCBI36 |
| NG_008318.1:g.14746C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456935.7:c.1444C>T MANE Select | ENSP00000395473.2:p.Arg482Trp | |
| ENST00000221363.8:c.1441C>T | ENSP00000221363.4:p.Arg481Trp | |
| ENST00000433513.5:n.50C>T | ||
| ENST00000456935.6:c.1444C>T | ENSP00000395473.2:p.Arg482Trp | |
| ENST00000466794.5:n.1343C>T | ||
| ENST00000495617.1:n.620C>T | ||
| ENST00000593686.1:c.54C>T | ||
| ENST00000595880.5:n.41C>T | ||
| NM_000528.3:c.1444C>T | NP_000519.2:p.Arg482Trp | |
| NM_001173498.1:c.1441C>T | NP_001166969.1:p.Arg481Trp | |
| XM_005259913.1:c.1447C>T | XP_005259970.1:p.Arg483Trp | |
| XM_011528017.1:c.343C>T | XP_011526319.1:p.Arg115Trp | |
| XM_005259913.2:c.1447C>T | XP_005259970.1:p.Arg483Trp | |
| XM_024451518.1:c.343C>T | XP_024307286.1:p.Arg115Trp | |
| NM_000528.4:c.1444C>T MANE Select | NP_000519.2:p.Arg482Trp | |
| NM_001173498.2:c.1441C>T | NP_001166969.1:p.Arg481Trp |