Canonical Allele Identifier: CA886690892

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1236391504
• gnomAD v3: 1-12208389-T-C
• gnomAD v4: 1-12208389-T-C
• MyVariant Identifiers: chr1:g.12268446T>C (hg19) ; chr1:g.12208389T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208389T>C , CM000663.2:g.12208389T>C	GRCh38
NC_000001.10:g.12268446T>C , CM000663.1:g.12268446T>C	GRCh37
NC_000001.9:g.12191033T>C	NCBI36
NG_029791.1:g.46387T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1369T>C MANE Select	ENSP00000365435.3:n.*1369T>C
ENST00000376259.6:c.*1369T>C	ENSP00000365435.3:n.*1369T>C
ENST00000492361.1:n.2744T>C
NM_001066.2:c.*1369T>C	NP_001057.1:n.*1369T>C
XM_011542060.1:c.*1369T>C	XP_011540362.1:n.*1369T>C
XM_011542061.1:c.*1369T>C	XP_011540363.1:n.*1369T>C
XM_011542062.1:c.2803T>C	XP_011540364.1:n.2803T>C
XM_011542063.1:c.*1369T>C	XP_011540365.1:n.*1369T>C
XM_011542060.2:c.*1369T>C	XP_011540362.1:n.*1369T>C
XM_011542063.2:c.*1369T>C	XP_011540365.1:n.*1369T>C
XM_017002214.1:c.*1369T>C	XP_016857703.1:n.*1369T>C
XM_017002215.1:c.*1369T>C	XP_016857704.1:n.*1369T>C
NM_001066.3:c.*1369T>C MANE Select	NP_001057.1:n.*1369T>C