Canonical Allele Identifier: CA1154001421

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192904C= , CM000663.2:g.12192904C=	GRCh38
NC_000001.10:g.12252961C= , CM000663.1:g.12252961C=	GRCh37
NC_000001.9:g.12175548C=	NCBI36
NG_029791.1:g.30902C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.593C= MANE Select	ENSP00000365435.3:p.Ala198=
ENST00000376259.6:c.593C=	ENSP00000365435.3:p.Ala198=
ENST00000489921.1:n.305C=
ENST00000492361.1:n.582C=
NM_001066.2:c.593C=	NP_001057.1:p.Ala198=
XM_011542060.1:c.593C=	XP_011540362.1:p.Ala198=
XM_011542061.1:c.593C=	XP_011540363.1:p.Ala198=
XM_011542062.1:c.572C=	XP_011540364.1:p.Ala191=
XM_011542063.1:c.593C=	XP_011540365.1:p.Ala198=
XM_011542060.2:c.593C=	XP_011540362.1:p.Ala198=
XM_011542063.2:c.593C=	XP_011540365.1:p.Ala198=
XM_017002211.1:c.593C=	XP_016857700.1:p.Ala198=
XM_017002214.1:c.8C=	XP_016857703.1:p.Ala3=
XM_017002215.1:c.8C=	XP_016857704.1:p.Ala3=
NM_001066.3:c.593C= MANE Select	NP_001057.1:p.Ala198=