Canonical Allele Identifier: CA18031587

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs187226764
• gnomAD v3: 1-12202840-G-A
• gnomAD v4: 1-12202840-G-A
• MyVariant Identifiers: chr1:g.12262897G>A (hg19) ; chr1:g.12202840G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202840G>A , CM000663.2:g.12202840G>A	GRCh38
NC_000001.10:g.12262897G>A , CM000663.1:g.12262897G>A	GRCh37
NC_000001.9:g.12185484G>A	NCBI36
NG_029791.1:g.40838G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+669G>A MANE Select	ENSP00000365435.3:n.1105+669G>A
ENST00000376259.6:c.1105+669G>A	ENSP00000365435.3:n.1105+669G>A
ENST00000492361.1:n.1094+669G>A
NM_001066.2:c.1105+669G>A	NP_001057.1:n.1105+669G>A
XM_011542060.1:c.1171+268G>A	XP_011540362.1:n.1171+268G>A
XM_011542061.1:c.1171+268G>A	XP_011540363.1:n.1171+268G>A
XM_011542062.1:c.1150+268G>A	XP_011540364.1:n.1150+268G>A
XM_011542063.1:c.1105+669G>A	XP_011540365.1:n.1105+669G>A
XM_011542060.2:c.1171+268G>A	XP_011540362.1:n.1171+268G>A
XM_011542063.2:c.1105+669G>A	XP_011540365.1:n.1105+669G>A
XM_017002214.1:c.586+268G>A	XP_016857703.1:n.586+268G>A
XM_017002215.1:c.520+669G>A	XP_016857704.1:n.520+669G>A
NM_001066.3:c.1105+669G>A MANE Select	NP_001057.1:n.1105+669G>A