Canonical Allele Identifier: CA886690886

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs970826991
• gnomAD v3: 1-12208360-C-T
• gnomAD v4: 1-12208360-C-T
• MyVariant Identifiers: chr1:g.12268417C>T (hg19) ; chr1:g.12208360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208360C>T , CM000663.2:g.12208360C>T	GRCh38
NC_000001.10:g.12268417C>T , CM000663.1:g.12268417C>T	GRCh37
NC_000001.9:g.12191004C>T	NCBI36
NG_029791.1:g.46358C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.*1340C>T MANE Select	ENSP00000365435.3:n.*1340C>T
ENST00000376259.6:c.*1340C>T	ENSP00000365435.3:n.*1340C>T
ENST00000492361.1:n.2715C>T
NM_001066.2:c.*1340C>T	NP_001057.1:n.*1340C>T
XM_011542060.1:c.*1340C>T	XP_011540362.1:n.*1340C>T
XM_011542061.1:c.*1340C>T	XP_011540363.1:n.*1340C>T
XM_011542062.1:c.2774C>T	XP_011540364.1:n.2774C>T
XM_011542063.1:c.*1340C>T	XP_011540365.1:n.*1340C>T
XM_011542060.2:c.*1340C>T	XP_011540362.1:n.*1340C>T
XM_011542063.2:c.*1340C>T	XP_011540365.1:n.*1340C>T
XM_017002214.1:c.*1340C>T	XP_016857703.1:n.*1340C>T
XM_017002215.1:c.*1340C>T	XP_016857704.1:n.*1340C>T
NM_001066.3:c.*1340C>T MANE Select	NP_001057.1:n.*1340C>T