Linked Data
ClinVar Variation Id:
2059129
dbSNP Id:
rs777637637
ExAC:
4:178359925 G / A
gnomAD v2:
4-178359925-G-A
gnomAD v3:
4-177438771-G-A
gnomAD v4:
4-177438771-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177438771G>A , CM000666.2:g.177438771G>A | GRCh38 |
| NC_000004.11:g.178359925G>A , CM000666.1:g.178359925G>A | GRCh37 |
| NC_000004.10:g.178596919G>A | NCBI36 |
| NG_011845.2:g.8733C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.7:c.481C>T MANE Select | ENSP00000264595.2:p.Arg161Trp | |
| ENST00000264595.6:c.481C>T | ENSP00000264595.2:p.Arg161Trp | |
| ENST00000502310.5:c.136C>T | ENSP00000423798.1:p.Arg46Trp | |
| ENST00000506853.5:n.515C>T | ||
| ENST00000510635.1:c.177C>T | ||
| ENST00000510955.5:n.402C>T | ||
| NM_000027.3:c.481C>T | NP_000018.2:p.Arg161Trp | |
| NM_001171988.1:c.481C>T | NP_001165459.1:p.Arg161Trp | |
| NR_033655.1:n.609C>T | ||
| XM_006714123.2:c.481C>T | XP_006714186.1:p.Arg161Trp | |
| XR_001741155.2:n.575C>T | ||
| NM_000027.4:c.481C>T MANE Select | NP_000018.2:p.Arg161Trp | |
| NM_001171988.2:c.481C>T | NP_001165459.1:p.Arg161Trp | |
| NR_033655.2:n.543C>T |