Linked Data
ClinVar Variation Id:
1445
dbSNP Id:
rs118204094
gnomAD v2:
11-118960701-C-T
gnomAD v3:
11-119089991-C-T
gnomAD v4:
11-119089991-C-T
PubMed:
PMID:8096492
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119089991C>T , CM000673.2:g.119089991C>T | GRCh38 |
| NC_000011.9:g.118960701C>T , CM000673.1:g.118960701C>T | GRCh37 |
| NC_000011.8:g.118465911C>T | NCBI36 |
| NG_008093.1:g.10115C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686218.1:c.181C>T | ENSP00000509288.1:p.Arg61Trp | |
| ENST00000686690.1:n.1196C>T | ||
| ENST00000691144.1:n.2087C>T | ||
| ENST00000691249.1:n.930C>T | ||
| ENST00000442944.7:c.328C>T | ENSP00000392041.3:p.Arg110Trp | |
| ENST00000534956.2:n.295C>T | ||
| ENST00000536813.6:c.295C>T | ENSP00000438726.2:p.Arg99Trp | |
| ENST00000546302.6:c.268C>T | ENSP00000445599.1:p.Arg90Trp | |
| ENST00000640813.1:c.295C>T | ENSP00000491061.1:p.Arg99Trp | |
| ENST00000648026.1:c.340C>T | ENSP00000498044.1:p.Arg114Trp | |
| ENST00000648374.1:c.295C>T | ENSP00000497255.1:p.Arg99Trp | |
| ENST00000648488.1:c.295C>T | ENSP00000498079.1:p.Arg99Trp | |
| ENST00000649823.1:n.563C>T | ||
| ENST00000649868.1:c.*54C>T | ENSP00000497548.1:n.*54C>T | |
| ENST00000650101.1:c.277C>T | ENSP00000496970.1:p.Arg93Trp | |
| ENST00000650307.1:n.1172C>T | ||
| ENST00000652429.1:c.346C>T MANE Select | ENSP00000498786.1:p.Arg116Trp | |
| ENST00000278715.7:c.346C>T | ENSP00000278715.3:p.Arg116Trp | |
| ENST00000392841.1:c.295C>T | ENSP00000376584.1:p.Arg99Trp | |
| ENST00000442944.6:c.295C>T | ENSP00000392041.2:p.Arg99Trp | |
| ENST00000534956.1:n.262C>T | ||
| ENST00000535253.5:c.295C>T | ENSP00000442079.1:p.Arg99Trp | |
| ENST00000535793.5:c.*241C>T | ENSP00000439904.1:n.*241C>T | |
| ENST00000536813.5:c.328C>T | ENSP00000438726.1:p.Arg110Trp | |
| ENST00000537841.5:c.295C>T | ENSP00000444730.1:p.Arg99Trp | |
| ENST00000539986.5:c.295C>T | ENSP00000440092.1:p.Arg99Trp | |
| ENST00000542044.5:n.791C>T | ||
| ENST00000542345.5:n.484C>T | ||
| ENST00000542729.5:c.295C>T | ENSP00000443058.1:p.Arg99Trp | |
| ENST00000542822.5:c.*282C>T | ENSP00000444817.1:n.*282C>T | |
| ENST00000543090.5:c.292C>T | ENSP00000445429.1:p.Arg98Trp | |
| ENST00000543543.5:n.581C>T | ||
| ENST00000543821.5:n.507C>T | ||
| ENST00000544360.5:n.314C>T | ||
| ENST00000544387.5:c.346C>T | ENSP00000438424.1:p.Arg116Trp | |
| ENST00000545621.5:c.*241C>T | ENSP00000444849.1:n.*241C>T | |
| ENST00000546226.5:n.634C>T | ||
| ENST00000546302.5:c.268C>T | ENSP00000445599.1:p.Arg90Trp | |
| NM_000190.3:c.346C>T | NP_000181.2:p.Arg116Trp | |
| NM_001024382.1:c.295C>T | NP_001019553.1:p.Arg99Trp | |
| NM_001258208.1:c.346C>T | NP_001245137.1:p.Arg116Trp | |
| NM_001258209.1:c.295C>T | NP_001245138.1:p.Arg99Trp | |
| XM_005271531.1:c.295C>T | XP_005271588.1:p.Arg99Trp | |
| XM_005271532.1:c.295C>T | XP_005271589.1:p.Arg99Trp | |
| XM_005271533.2:c.292C>T | XP_005271590.1:p.Arg98Trp | |
| XM_011542796.1:c.181C>T | XP_011541098.1:p.Arg61Trp | |
| NM_000190.4:c.346C>T MANE Select | NP_000181.2:p.Arg116Trp | |
| NM_001024382.2:c.295C>T | NP_001019553.1:p.Arg99Trp | |
| XM_005271533.3:c.292C>T | XP_005271590.1:p.Arg98Trp | |
| XM_017017629.1:c.295C>T | XP_016873118.1:p.Arg99Trp | |
| XM_024448460.1:c.292C>T | XP_024304228.1:p.Arg98Trp | |
| NM_001258208.2:c.346C>T | NP_001245137.1:p.Arg116Trp | |
| NM_001258209.2:c.295C>T | NP_001245138.1:p.Arg99Trp |