Canonical Allele Identifier: CA2643342695

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12208522-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208522C>A , CM000663.2:g.12208522C>A	GRCh38
NC_000001.10:g.12268579C>A , CM000663.1:g.12268579C>A	GRCh37
NC_000001.9:g.12191166C>A	NCBI36
NG_029791.1:g.46520C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1502C>A MANE Select	ENSP00000365435.3:n.*1502C>A
ENST00000376259.6:c.*1502C>A	ENSP00000365435.3:n.*1502C>A
ENST00000492361.1:n.2877C>A
NM_001066.2:c.*1502C>A	NP_001057.1:n.*1502C>A
XM_011542060.1:c.*1502C>A	XP_011540362.1:n.*1502C>A
XM_011542061.1:c.*1502C>A	XP_011540363.1:n.*1502C>A
XM_011542062.1:c.2936C>A	XP_011540364.1:n.2936C>A
XM_011542063.1:c.*1502C>A	XP_011540365.1:n.*1502C>A
XM_011542060.2:c.*1502C>A	XP_011540362.1:n.*1502C>A
XM_011542063.2:c.*1502C>A	XP_011540365.1:n.*1502C>A
XM_017002214.1:c.*1502C>A	XP_016857703.1:n.*1502C>A
XM_017002215.1:c.*1502C>A	XP_016857704.1:n.*1502C>A
NM_001066.3:c.*1502C>A MANE Select	NP_001057.1:n.*1502C>A