Canonical Allele Identifier: CA886685506

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1417489393
• gnomAD v3: 1-12202801-G-C
• gnomAD v4: 1-12202801-G-C
• MyVariant Identifiers: chr1:g.12262858G>C (hg19) ; chr1:g.12202801G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202801G>C , CM000663.2:g.12202801G>C	GRCh38
NC_000001.10:g.12262858G>C , CM000663.1:g.12262858G>C	GRCh37
NC_000001.9:g.12185445G>C	NCBI36
NG_029791.1:g.40799G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+630G>C MANE Select	ENSP00000365435.3:n.1105+630G>C
ENST00000376259.6:c.1105+630G>C	ENSP00000365435.3:n.1105+630G>C
ENST00000492361.1:n.1094+630G>C
NM_001066.2:c.1105+630G>C	NP_001057.1:n.1105+630G>C
XM_011542060.1:c.1171+229G>C	XP_011540362.1:n.1171+229G>C
XM_011542061.1:c.1171+229G>C	XP_011540363.1:n.1171+229G>C
XM_011542062.1:c.1150+229G>C	XP_011540364.1:n.1150+229G>C
XM_011542063.1:c.1105+630G>C	XP_011540365.1:n.1105+630G>C
XM_011542060.2:c.1171+229G>C	XP_011540362.1:n.1171+229G>C
XM_011542063.2:c.1105+630G>C	XP_011540365.1:n.1105+630G>C
XM_017002214.1:c.586+229G>C	XP_016857703.1:n.586+229G>C
XM_017002215.1:c.520+630G>C	XP_016857704.1:n.520+630G>C
NM_001066.3:c.1105+630G>C MANE Select	NP_001057.1:n.1105+630G>C