Canonical Allele Identifier: CA338455026

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252964T>A (hg19) ; chr1:g.12192907T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192907T>A , CM000663.2:g.12192907T>A	GRCh38
NC_000001.10:g.12252964T>A , CM000663.1:g.12252964T>A	GRCh37
NC_000001.9:g.12175551T>A	NCBI36
NG_029791.1:g.30905T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.596T>A MANE Select	ENSP00000365435.3:p.Val199Asp
ENST00000376259.6:c.596T>A	ENSP00000365435.3:p.Val199Asp
ENST00000489921.1:n.308T>A
ENST00000492361.1:n.585T>A
NM_001066.2:c.596T>A	NP_001057.1:p.Val199Asp
XM_011542060.1:c.596T>A	XP_011540362.1:p.Val199Asp
XM_011542061.1:c.596T>A	XP_011540363.1:p.Val199Asp
XM_011542062.1:c.575T>A	XP_011540364.1:p.Val192Asp
XM_011542063.1:c.596T>A	XP_011540365.1:p.Val199Asp
XM_011542060.2:c.596T>A	XP_011540362.1:p.Val199Asp
XM_011542063.2:c.596T>A	XP_011540365.1:p.Val199Asp
XM_017002211.1:c.596T>A	XP_016857700.1:p.Val199Asp
XM_017002214.1:c.11T>A	XP_016857703.1:p.Val4Asp
XM_017002215.1:c.11T>A	XP_016857704.1:p.Val4Asp
NM_001066.3:c.596T>A MANE Select	NP_001057.1:p.Val199Asp