Canonical Allele Identifier: CA126289
Gene: FSHB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16242
ClinVar RCV Id: RCV000017629
dbSNP Id: rs121909666

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.30233692C>A , CM000673.2:g.30233692C>A GRCh38
NC_000011.8:g.30211815C>A NCBI36
NC_000011.9:g.30255239C>A , CM000673.1:g.30255239C>A GRCh37
NG_008144.1:g.7677C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000254122.7:c.282C>A ENSP00000254122.3:p.Tyr94Ter
ENST00000417547.1:c.282C>A ENSP00000416606.1:p.Tyr94Ter
ENST00000533718.1:c.282C>A ENSP00000433424.1:p.Tyr94Ter
NM_000510.2:c.282C>A VV NP_000501.1:p.Tyr94Ter
NM_001018080.1:c.282C>A VV NP_001018090.1:p.Tyr94Ter
XM_011519964.1:c.282C>A XP_011518266.1:p.Tyr94Ter
XR_931152.1:n.463+83198G>T
XR_931153.1:n.284+83198G>T