Canonical Allele Identifier: CA10831910
Gene: TNFRSF1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1061631

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208442G>A , CM000663.2:g.12208442G>A GRCh38
NC_000001.9:g.12191086G>A NCBI36
NC_000001.10:g.12268499G>A , CM000663.1:g.12268499G>A GRCh37
NG_029791.1:g.46440G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.6:c.*1422G>A ENSP00000365435.3:p.=
ENST00000492361.1:n.2797G>A
NM_001066.2:c.*1422G>A NP_001057.1:p.=
XM_011542060.1:c.*1422G>A XP_011540362.1:p.=
XM_011542061.1:c.*1422G>A XP_011540363.1:p.=
XM_011542062.1:n.2856G>A XP_011540364.1:p.=
XM_011542063.1:c.*1422G>A XP_011540365.1:p.=