Canonical Allele Identifier: CA1139849755
Gene: TNFRSF1B HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.*1422G= MANE Select ENSP00000365435.3:n.*1422G=
ENST00000376259.6:c.*1422G= ENSP00000365435.3:n.*1422G=
ENST00000492361.1:n.2797G=
NM_001066.2:c.*1422G= NP_001057.1:n.*1422G=
XM_011542060.1:c.*1422G= XP_011540362.1:n.*1422G=
XM_011542061.1:c.*1422G= XP_011540363.1:n.*1422G=
XM_011542062.1:c.2856G= XP_011540364.1:n.2856G=
XM_011542063.1:c.*1422G= XP_011540365.1:n.*1422G=
XM_011542060.2:c.*1422G= XP_011540362.1:n.*1422G=
XM_011542063.2:c.*1422G= XP_011540365.1:n.*1422G=
XM_017002214.1:c.*1422G= XP_016857703.1:n.*1422G=
XM_017002215.1:c.*1422G= XP_016857704.1:n.*1422G=
NM_001066.3:c.*1422G= MANE Select NP_001057.1:n.*1422G=