Canonical Allele Identifier: CA2838196483

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12188918T>A , CM000663.2:g.12188918T>A	GRCh38
NC_000001.10:g.12248975T>A , CM000663.1:g.12248975T>A	GRCh37
NC_000001.9:g.12171562T>A	NCBI36
NG_029791.1:g.26916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.178+23T>A MANE Select	ENSP00000365435.3:n.178+23T>A
ENST00000376259.6:c.178+23T>A	ENSP00000365435.3:n.178+23T>A
ENST00000492361.1:n.168-2039T>A
ENST00000536782.2:c.178+23T>A	ENSP00000440425.1:n.178+23T>A
NM_001066.2:c.178+23T>A	NP_001057.1:n.178+23T>A
XM_011542060.1:c.178+23T>A	XP_011540362.1:n.178+23T>A
XM_011542061.1:c.178+23T>A	XP_011540363.1:n.178+23T>A
XM_011542062.1:c.157+23T>A	XP_011540364.1:n.157+23T>A
XM_011542063.1:c.178+23T>A	XP_011540365.1:n.178+23T>A
XM_011542060.2:c.178+23T>A	XP_011540362.1:n.178+23T>A
XM_011542063.2:c.178+23T>A	XP_011540365.1:n.178+23T>A
XM_017002211.1:c.178+23T>A	XP_016857700.1:n.178+23T>A
XM_017002214.1:c.-407-2039T>A	XP_016857703.1:n.-407-2039T>A
XM_017002215.1:c.-407-2039T>A	XP_016857704.1:n.-407-2039T>A
NM_001066.3:c.178+23T>A MANE Select	NP_001057.1:n.178+23T>A