Linked Data
ClinVar Variation Id:
161251
dbSNP Id:
rs34413634
ExAC:
11:118962207 C / T
gnomAD v3:
11-119091497-C-T
gnomAD v4:
11-119091497-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119091497C>T , CM000673.2:g.119091497C>T | GRCh38 |
| NC_000011.9:g.118962207C>T , CM000673.1:g.118962207C>T | GRCh37 |
| NC_000011.8:g.118467417C>T | NCBI36 |
| NG_008093.1:g.11621C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686218.1:c.418C>T | ENSP00000509288.1:p.Arg140Cys | |
| ENST00000686690.1:n.1433C>T | ||
| ENST00000691144.1:n.2324C>T | ||
| ENST00000691249.1:n.1167C>T | ||
| ENST00000442944.7:c.565C>T | ENSP00000392041.3:p.Arg189Cys | |
| ENST00000534956.2:n.448-364C>T | ||
| ENST00000536813.6:c.532C>T | ENSP00000438726.2:p.Arg178Cys | |
| ENST00000546302.6:c.505C>T | ENSP00000445599.1:p.Arg169Cys | |
| ENST00000640813.1:c.448-364C>T | ENSP00000491061.1:n.448-364C>T | |
| ENST00000648026.1:c.493-364C>T | ENSP00000498044.1:n.493-364C>T | |
| ENST00000648374.1:c.532C>T | ENSP00000497255.1:p.Arg178Cys | |
| ENST00000648488.1:c.*85+241C>T | ENSP00000498079.1:n.*85+241C>T | |
| ENST00000649823.1:n.800C>T | ||
| ENST00000649868.1:c.*207-364C>T | ENSP00000497548.1:n.*207-364C>T | |
| ENST00000650101.1:c.514C>T | ENSP00000496970.1:p.Arg172Cys | |
| ENST00000650307.1:n.1409C>T | ||
| ENST00000652429.1:c.583C>T MANE Select | ENSP00000498786.1:p.Arg195Cys | |
| ENST00000278715.7:c.583C>T | ENSP00000278715.3:p.Arg195Cys | |
| ENST00000392841.1:c.532C>T | ENSP00000376584.1:p.Arg178Cys | |
| ENST00000442944.6:c.532C>T | ENSP00000392041.2:p.Arg178Cys | |
| ENST00000534956.1:n.415-364C>T | ||
| ENST00000535253.5:c.532C>T | ENSP00000442079.1:p.Arg178Cys | |
| ENST00000535793.5:c.*478C>T | ENSP00000439904.1:n.*478C>T | |
| ENST00000537841.5:c.532C>T | ENSP00000444730.1:p.Arg178Cys | |
| ENST00000539986.5:c.532C>T | ENSP00000440092.1:p.Arg178Cys | |
| ENST00000542044.5:n.1028C>T | ||
| ENST00000542345.5:n.721C>T | ||
| ENST00000542729.5:c.532C>T | ENSP00000443058.1:p.Arg178Cys | |
| ENST00000542822.5:c.*519C>T | ENSP00000444817.1:n.*519C>T | |
| ENST00000543090.5:c.529C>T | ENSP00000445429.1:p.Arg177Cys | |
| ENST00000543543.5:n.818C>T | ||
| ENST00000544360.5:n.551C>T | ||
| ENST00000544387.5:c.583C>T | ENSP00000438424.1:p.Arg195Cys | |
| ENST00000545621.5:c.*478C>T | ENSP00000444849.1:n.*478C>T | |
| ENST00000546226.5:n.871C>T | ||
| ENST00000546302.5:c.505C>T | ENSP00000445599.1:p.Arg169Cys | |
| NM_000190.3:c.583C>T | NP_000181.2:p.Arg195Cys | |
| NM_001024382.1:c.532C>T | NP_001019553.1:p.Arg178Cys | |
| NM_001258208.1:c.583C>T | NP_001245137.1:p.Arg195Cys | |
| NM_001258209.1:c.532C>T | NP_001245138.1:p.Arg178Cys | |
| XM_005271531.1:c.532C>T | XP_005271588.1:p.Arg178Cys | |
| XM_005271532.1:c.532C>T | XP_005271589.1:p.Arg178Cys | |
| XM_005271533.2:c.529C>T | XP_005271590.1:p.Arg177Cys | |
| XM_011542796.1:c.418C>T | XP_011541098.1:p.Arg140Cys | |
| NM_000190.4:c.583C>T MANE Select | NP_000181.2:p.Arg195Cys | |
| NM_001024382.2:c.532C>T | NP_001019553.1:p.Arg178Cys | |
| XM_005271533.3:c.529C>T | XP_005271590.1:p.Arg177Cys | |
| XM_017017629.1:c.532C>T | XP_016873118.1:p.Arg178Cys | |
| XM_024448460.1:c.529C>T | XP_024304228.1:p.Arg177Cys | |
| NM_001258208.2:c.583C>T | NP_001245137.1:p.Arg195Cys | |
| NM_001258209.2:c.532C>T | NP_001245138.1:p.Arg178Cys |