Canonical Allele Identifier: CA1154001328

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192714G= , CM000663.2:g.12192714G=	GRCh38
NC_000001.10:g.12252771G= , CM000663.1:g.12252771G=	GRCh37
NC_000001.9:g.12175358G=	NCBI36
NG_029791.1:g.30712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-149G= MANE Select	ENSP00000365435.3:n.552-149G=
ENST00000376259.6:c.552-149G=	ENSP00000365435.3:n.552-149G=
ENST00000489921.1:n.264-149G=
ENST00000492361.1:n.541-149G=
NM_001066.2:c.552-149G=	NP_001057.1:n.552-149G=
XM_011542060.1:c.552-149G=	XP_011540362.1:n.552-149G=
XM_011542061.1:c.552-149G=	XP_011540363.1:n.552-149G=
XM_011542062.1:c.531-149G=	XP_011540364.1:n.531-149G=
XM_011542063.1:c.552-149G=	XP_011540365.1:n.552-149G=
XM_011542060.2:c.552-149G=	XP_011540362.1:n.552-149G=
XM_011542063.2:c.552-149G=	XP_011540365.1:n.552-149G=
XM_017002211.1:c.552-149G=	XP_016857700.1:n.552-149G=
XM_017002214.1:c.-34-149G=	XP_016857703.1:n.-34-149G=
XM_017002215.1:c.-34-149G=	XP_016857704.1:n.-34-149G=
NM_001066.3:c.552-149G= MANE Select	NP_001057.1:n.552-149G=