Canonical Allele Identifier: CA18037341

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs11807940
• MyVariant Identifiers: chr1:g.12268342C>T (hg19) ; chr1:g.12208285C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208285C>T , CM000663.2:g.12208285C>T	GRCh38
NC_000001.10:g.12268342C>T , CM000663.1:g.12268342C>T	GRCh37
NC_000001.9:g.12190929C>T	NCBI36
NG_029791.1:g.46283C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1265C>T MANE Select	ENSP00000365435.3:n.*1265C>T
ENST00000376259.6:c.*1265C>T	ENSP00000365435.3:n.*1265C>T
ENST00000492361.1:n.2640C>T
NM_001066.2:c.*1265C>T	NP_001057.1:n.*1265C>T
XM_011542060.1:c.*1265C>T	XP_011540362.1:n.*1265C>T
XM_011542061.1:c.*1265C>T	XP_011540363.1:n.*1265C>T
XM_011542062.1:c.2699C>T	XP_011540364.1:n.2699C>T
XM_011542063.1:c.*1265C>T	XP_011540365.1:n.*1265C>T
XM_011542060.2:c.*1265C>T	XP_011540362.1:n.*1265C>T
XM_011542063.2:c.*1265C>T	XP_011540365.1:n.*1265C>T
XM_017002214.1:c.*1265C>T	XP_016857703.1:n.*1265C>T
XM_017002215.1:c.*1265C>T	XP_016857704.1:n.*1265C>T
NM_001066.3:c.*1265C>T MANE Select	NP_001057.1:n.*1265C>T