Linked Data
ClinVar Variation Id:
4590
ClinVar RCV Id:
RCV001558568
dbSNP Id:
rs121908173
ExAC:
20:45354069 C / T
gnomAD v2:
20-45354069-C-T
gnomAD v3:
20-46725430-C-T
gnomAD v4:
20-46725430-C-T
COSMIC:
COSM5037414
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46725430C>T , CM000682.2:g.46725430C>T | GRCh38 |
| NC_000020.10:g.45354069C>T , CM000682.1:g.45354069C>T | GRCh37 |
| NC_000020.9:g.44787476C>T | NCBI36 |
| NG_016284.1:g.20791C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359271.4:c.394C>T MANE Select | ENSP00000352216.2:p.Arg132Trp | |
| ENST00000359271.3:c.394C>T | ENSP00000352216.2:p.Arg132Trp | |
| ENST00000611837.1:n.546C>T | ||
| NM_030777.3:c.394C>T | NP_110404.1:p.Arg132Trp | |
| XM_011529060.1:c.457C>T | XP_011527362.1:p.Arg153Trp | |
| XM_011529061.1:c.403C>T | XP_011527363.1:p.Arg135Trp | |
| XM_011529062.1:c.457C>T | XP_011527364.1:p.Arg153Trp | |
| XM_011529063.1:c.457C>T | XP_011527365.1:p.Arg153Trp | |
| XM_011529064.1:c.457C>T | XP_011527366.1:p.Arg153Trp | |
| XM_011529065.1:c.457C>T | XP_011527367.1:p.Arg153Trp | |
| XR_936641.1:n.593C>T | ||
| XM_011529060.2:c.457C>T | XP_011527362.1:p.Arg153Trp | |
| XM_011529061.2:c.403C>T | XP_011527363.1:p.Arg135Trp | |
| XM_011529062.2:c.457C>T | XP_011527364.1:p.Arg153Trp | |
| XM_011529063.2:c.457C>T | XP_011527365.1:p.Arg153Trp | |
| XM_011529064.2:c.457C>T | XP_011527366.1:p.Arg153Trp | |
| XM_011529065.2:c.457C>T | XP_011527367.1:p.Arg153Trp | |
| XM_017028087.2:c.394C>T | XP_016883576.1:p.Arg132Trp | |
| XR_936641.2:n.580C>T | ||
| NM_030777.4:c.394C>T MANE Select | NP_110404.1:p.Arg132Trp |