Canonical Allele Identifier: CA1144144349

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202782G= , CM000663.2:g.12202782G=	GRCh38
NC_000001.10:g.12262839G= , CM000663.1:g.12262839G=	GRCh37
NC_000001.9:g.12185426G=	NCBI36
NG_029791.1:g.40780G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.1105+611G= MANE Select	ENSP00000365435.3:n.1105+611G=
ENST00000376259.6:c.1105+611G=	ENSP00000365435.3:n.1105+611G=
ENST00000492361.1:n.1094+611G=
NM_001066.2:c.1105+611G=	NP_001057.1:n.1105+611G=
XM_011542060.1:c.1171+210G=	XP_011540362.1:n.1171+210G=
XM_011542061.1:c.1171+210G=	XP_011540363.1:n.1171+210G=
XM_011542062.1:c.1150+210G=	XP_011540364.1:n.1150+210G=
XM_011542063.1:c.1105+611G=	XP_011540365.1:n.1105+611G=
XM_011542060.2:c.1171+210G=	XP_011540362.1:n.1171+210G=
XM_011542063.2:c.1105+611G=	XP_011540365.1:n.1105+611G=
XM_017002214.1:c.586+210G=	XP_016857703.1:n.586+210G=
XM_017002215.1:c.520+611G=	XP_016857704.1:n.520+611G=
NM_001066.3:c.1105+611G= MANE Select	NP_001057.1:n.1105+611G=