Canonical Allele Identifier: CA2742495726

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208756G>A , CM000663.2:g.12208756G>A	GRCh38
NC_000001.10:g.12268813G>A , CM000663.1:g.12268813G>A	GRCh37
NC_000001.9:g.12191400G>A	NCBI36
NG_029791.1:g.46754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1736G>A MANE Select	ENSP00000365435.3:n.*1736G>A
ENST00000376259.6:c.*1736G>A	ENSP00000365435.3:n.*1736G>A
ENST00000492361.1:n.3111G>A
NM_001066.2:c.*1736G>A	NP_001057.1:n.*1736G>A
XM_011542060.1:c.*1736G>A	XP_011540362.1:n.*1736G>A
XM_011542061.1:c.*1736G>A	XP_011540363.1:n.*1736G>A
XM_011542062.1:c.3170G>A	XP_011540364.1:n.3170G>A
XM_011542063.1:c.*1736G>A	XP_011540365.1:n.*1736G>A
XM_011542060.2:c.*1736G>A	XP_011540362.1:n.*1736G>A
XM_011542063.2:c.*1736G>A	XP_011540365.1:n.*1736G>A
XM_017002214.1:c.*1736G>A	XP_016857703.1:n.*1736G>A
XM_017002215.1:c.*1736G>A	XP_016857704.1:n.*1736G>A
NM_001066.3:c.*1736G>A MANE Select	NP_001057.1:n.*1736G>A