Canonical Allele Identifier: CA1154007842
Gene: TNFRSF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208263G= , CM000663.2:g.12208263G= GRCh38
NC_000001.10:g.12268320G= , CM000663.1:g.12268320G= GRCh37
NC_000001.9:g.12190907G= NCBI36
NG_029791.1:g.46261G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376259.7:c.*1243G= MANE Select ENSP00000365435.3:n.*1243G=
ENST00000376259.6:c.*1243G= ENSP00000365435.3:n.*1243G=
ENST00000492361.1:n.2618G=
NM_001066.2:c.*1243G= NP_001057.1:n.*1243G=
XM_011542060.1:c.*1243G= XP_011540362.1:n.*1243G=
XM_011542061.1:c.*1243G= XP_011540363.1:n.*1243G=
XM_011542062.1:c.2677G= XP_011540364.1:n.2677G=
XM_011542063.1:c.*1243G= XP_011540365.1:n.*1243G=
XM_011542060.2:c.*1243G= XP_011540362.1:n.*1243G=
XM_011542063.2:c.*1243G= XP_011540365.1:n.*1243G=
XM_017002214.1:c.*1243G= XP_016857703.1:n.*1243G=
XM_017002215.1:c.*1243G= XP_016857704.1:n.*1243G=
NM_001066.3:c.*1243G= MANE Select NP_001057.1:n.*1243G=