Canonical Allele Identifier: CA1154007952
Gene: TNFRSF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208504A= , CM000663.2:g.12208504A= GRCh38
NC_000001.10:g.12268561A= , CM000663.1:g.12268561A= GRCh37
NC_000001.9:g.12191148A= NCBI36
NG_029791.1:g.46502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376259.7:c.*1484A= MANE Select ENSP00000365435.3:n.*1484A=
ENST00000376259.6:c.*1484A= ENSP00000365435.3:n.*1484A=
ENST00000492361.1:n.2859A=
NM_001066.2:c.*1484A= NP_001057.1:n.*1484A=
XM_011542060.1:c.*1484A= XP_011540362.1:n.*1484A=
XM_011542061.1:c.*1484A= XP_011540363.1:n.*1484A=
XM_011542062.1:c.2918A= XP_011540364.1:n.2918A=
XM_011542063.1:c.*1484A= XP_011540365.1:n.*1484A=
XM_011542060.2:c.*1484A= XP_011540362.1:n.*1484A=
XM_011542063.2:c.*1484A= XP_011540365.1:n.*1484A=
XM_017002214.1:c.*1484A= XP_016857703.1:n.*1484A=
XM_017002215.1:c.*1484A= XP_016857704.1:n.*1484A=
NM_001066.3:c.*1484A= MANE Select NP_001057.1:n.*1484A=