Linked Data
ClinVar Variation Id:
4589
dbSNP Id:
rs121908172
ExAC:
20:45354951 G / T
gnomAD v2:
20-45354951-G-T
gnomAD v3:
20-46726312-G-T
gnomAD v4:
20-46726312-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46726312G>T , CM000682.2:g.46726312G>T | GRCh38 |
| NC_000020.10:g.45354951G>T , CM000682.1:g.45354951G>T | GRCh37 |
| NC_000020.9:g.44788358G>T | NCBI36 |
| NG_016284.1:g.21673G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359271.4:c.1276G>T MANE Select | ENSP00000352216.2:p.Gly426Trp | |
| ENST00000359271.3:c.1276G>T | ENSP00000352216.2:p.Gly426Trp | |
| NM_030777.3:c.1276G>T | NP_110404.1:p.Gly426Trp | |
| XM_011529060.1:c.1339G>T | XP_011527362.1:p.Gly447Trp | |
| XM_011529061.1:c.1285G>T | XP_011527363.1:p.Gly429Trp | |
| XM_011529062.1:c.1339G>T | XP_011527364.1:p.Gly447Trp | |
| XM_011529063.1:c.1339G>T | XP_011527365.1:p.Gly447Trp | |
| XM_011529064.1:c.1339G>T | XP_011527366.1:p.Gly447Trp | |
| XM_011529065.1:c.1339G>T | XP_011527367.1:p.Gly447Trp | |
| XR_936641.1:n.1475G>T | ||
| XM_011529060.2:c.1339G>T | XP_011527362.1:p.Gly447Trp | |
| XM_011529061.2:c.1285G>T | XP_011527363.1:p.Gly429Trp | |
| XM_011529062.2:c.1339G>T | XP_011527364.1:p.Gly447Trp | |
| XM_011529063.2:c.1339G>T | XP_011527365.1:p.Gly447Trp | |
| XM_011529064.2:c.1339G>T | XP_011527366.1:p.Gly447Trp | |
| XM_011529065.2:c.1339G>T | XP_011527367.1:p.Gly447Trp | |
| XM_017028087.2:c.1276G>T | XP_016883576.1:p.Gly426Trp | |
| XR_936641.2:n.1462G>T | ||
| NM_030777.4:c.1276G>T MANE Select | NP_110404.1:p.Gly426Trp |