Canonical Allele Identifier: CA886690948

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1451296627
• MyVariant Identifiers: chr1:g.12268528T>A (hg19) ; chr1:g.12208471T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208471T>A , CM000663.2:g.12208471T>A	GRCh38
NC_000001.10:g.12268528T>A , CM000663.1:g.12268528T>A	GRCh37
NC_000001.9:g.12191115T>A	NCBI36
NG_029791.1:g.46469T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.*1451T>A MANE Select	ENSP00000365435.3:n.*1451T>A
ENST00000376259.6:c.*1451T>A	ENSP00000365435.3:n.*1451T>A
ENST00000492361.1:n.2826T>A
NM_001066.2:c.*1451T>A	NP_001057.1:n.*1451T>A
XM_011542060.1:c.*1451T>A	XP_011540362.1:n.*1451T>A
XM_011542061.1:c.*1451T>A	XP_011540363.1:n.*1451T>A
XM_011542062.1:c.2885T>A	XP_011540364.1:n.2885T>A
XM_011542063.1:c.*1451T>A	XP_011540365.1:n.*1451T>A
XM_011542060.2:c.*1451T>A	XP_011540362.1:n.*1451T>A
XM_011542063.2:c.*1451T>A	XP_011540365.1:n.*1451T>A
XM_017002214.1:c.*1451T>A	XP_016857703.1:n.*1451T>A
XM_017002215.1:c.*1451T>A	XP_016857704.1:n.*1451T>A
NM_001066.3:c.*1451T>A MANE Select	NP_001057.1:n.*1451T>A