Linked Data
dbSNP Id:
rs750689462
ExAC:
14:81610587 A / T
gnomAD v2:
14-81610587-A-T
gnomAD v4:
14-81144243-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.81144243A>T , CM000676.2:g.81144243A>T | GRCh38 |
| NC_000014.8:g.81610587A>T , CM000676.1:g.81610587A>T | GRCh37 |
| NC_000014.7:g.80680340A>T | NCBI36 |
| NG_009206.1:g.193719A>T , LRG_523:g.193719A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298171.7:c.2185A>T MANE Select | ENSP00000298171.2:p.Arg729Trp | |
| ENST00000637447.1:c.1088A>T | ||
| ENST00000298171.6:c.2185A>T | ENSP00000298171.2:p.Arg729Trp | |
| ENST00000541158.6:c.2185A>T | ENSP00000441235.2:p.Arg729Trp | |
| NM_000369.2:c.2185A>T , LRG_523t1:c.2185A>T | NP_000360.2:p.Arg729Trp | |
| XM_005268037.3:c.2185A>T | XP_005268094.1:p.Arg729Trp | |
| XM_011537119.1:c.1906A>T | XP_011535421.1:p.Arg636Trp | |
| XR_245790.3:n.2086+20950T>A | ||
| XR_429385.2:n.853+20950T>A | ||
| XR_429386.2:n.854+20950T>A | ||
| XR_944075.1:n.865+20950T>A | ||
| XR_944076.1:n.861+20950T>A | ||
| XR_944077.1:n.865+20950T>A | ||
| XR_944078.1:n.865+20950T>A | ||
| XR_944079.1:n.855+20950T>A | ||
| XM_005268037.4:c.2185A>T | XP_005268094.1:p.Arg729Trp | |
| XM_011537119.2:c.1906A>T | XP_011535421.1:p.Arg636Trp | |
| XR_001751021.1:n.2753+20950T>A | ||
| XR_001751022.1:n.2753+20950T>A | ||
| XR_001751023.1:n.2753+20950T>A | ||
| XR_944075.3:n.929+20950T>A | ||
| NM_000369.4:c.2185A>T | NP_000360.2:p.Arg729Trp | |
| NM_000369.5:c.2185A>T MANE Select | NP_000360.2:p.Arg729Trp |