Canonical Allele Identifier: CA338455291

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1639181821
• gnomAD v3: 1-12192940-C-T
• gnomAD v4: 1-12192940-C-T
• MyVariant Identifiers: chr1:g.12252997C>T (hg19) ; chr1:g.12192940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192940C>T , CM000663.2:g.12192940C>T	GRCh38
NC_000001.10:g.12252997C>T , CM000663.1:g.12252997C>T	GRCh37
NC_000001.9:g.12175584C>T	NCBI36
NG_029791.1:g.30938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.629C>T MANE Select	ENSP00000365435.3:p.Ala210Val
ENST00000376259.6:c.629C>T	ENSP00000365435.3:p.Ala210Val
ENST00000489921.1:n.341C>T
ENST00000492361.1:n.618C>T
NM_001066.2:c.629C>T	NP_001057.1:p.Ala210Val
XM_011542060.1:c.629C>T	XP_011540362.1:p.Ala210Val
XM_011542061.1:c.629C>T	XP_011540363.1:p.Ala210Val
XM_011542062.1:c.608C>T	XP_011540364.1:p.Ala203Val
XM_011542063.1:c.629C>T	XP_011540365.1:p.Ala210Val
XM_011542060.2:c.629C>T	XP_011540362.1:p.Ala210Val
XM_011542063.2:c.629C>T	XP_011540365.1:p.Ala210Val
XM_017002211.1:c.629C>T	XP_016857700.1:p.Ala210Val
XM_017002214.1:c.44C>T	XP_016857703.1:p.Ala15Val
XM_017002215.1:c.44C>T	XP_016857704.1:p.Ala15Val
NM_001066.3:c.629C>T MANE Select	NP_001057.1:p.Ala210Val