Canonical Allele Identifier: CA1146297509

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192822T= , CM000663.2:g.12192822T=	GRCh38
NC_000001.10:g.12252879T= , CM000663.1:g.12252879T=	GRCh37
NC_000001.9:g.12175466T=	NCBI36
NG_029791.1:g.30820T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-41T= MANE Select	ENSP00000365435.3:n.552-41T=
ENST00000376259.6:c.552-41T=	ENSP00000365435.3:n.552-41T=
ENST00000489921.1:n.264-41T=
ENST00000492361.1:n.541-41T=
NM_001066.2:c.552-41T=	NP_001057.1:n.552-41T=
XM_011542060.1:c.552-41T=	XP_011540362.1:n.552-41T=
XM_011542061.1:c.552-41T=	XP_011540363.1:n.552-41T=
XM_011542062.1:c.531-41T=	XP_011540364.1:n.531-41T=
XM_011542063.1:c.552-41T=	XP_011540365.1:n.552-41T=
XM_011542060.2:c.552-41T=	XP_011540362.1:n.552-41T=
XM_011542063.2:c.552-41T=	XP_011540365.1:n.552-41T=
XM_017002211.1:c.552-41T=	XP_016857700.1:n.552-41T=
XM_017002214.1:c.-34-41T=	XP_016857703.1:n.-34-41T=
XM_017002215.1:c.-34-41T=	XP_016857704.1:n.-34-41T=
NM_001066.3:c.552-41T= MANE Select	NP_001057.1:n.552-41T=