Canonical Allele Identifier: CA1140055781
Gene: TNFRSF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12202735A= , CM000663.2:g.12202735A= GRCh38
NC_000001.10:g.12262792A= , CM000663.1:g.12262792A= GRCh37
NC_000001.9:g.12185379A= NCBI36
NG_029791.1:g.40733A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376259.7:c.1105+564A= MANE Select ENSP00000365435.3:n.1105+564A=
ENST00000376259.6:c.1105+564A= ENSP00000365435.3:n.1105+564A=
ENST00000492361.1:n.1094+564A=
NM_001066.2:c.1105+564A= NP_001057.1:n.1105+564A=
XM_011542060.1:c.1171+163A= XP_011540362.1:n.1171+163A=
XM_011542061.1:c.1171+163A= XP_011540363.1:n.1171+163A=
XM_011542062.1:c.1150+163A= XP_011540364.1:n.1150+163A=
XM_011542063.1:c.1105+564A= XP_011540365.1:n.1105+564A=
XM_011542060.2:c.1171+163A= XP_011540362.1:n.1171+163A=
XM_011542063.2:c.1105+564A= XP_011540365.1:n.1105+564A=
XM_017002214.1:c.586+163A= XP_016857703.1:n.586+163A=
XM_017002215.1:c.520+564A= XP_016857704.1:n.520+564A=
NM_001066.3:c.1105+564A= MANE Select NP_001057.1:n.1105+564A=