Canonical Allele Identifier: CA1145960213

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202800A= , CM000663.2:g.12202800A=	GRCh38
NC_000001.10:g.12262857A= , CM000663.1:g.12262857A=	GRCh37
NC_000001.9:g.12185444A=	NCBI36
NG_029791.1:g.40798A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.1105+629A= MANE Select	ENSP00000365435.3:n.1105+629A=
ENST00000376259.6:c.1105+629A=	ENSP00000365435.3:n.1105+629A=
ENST00000492361.1:n.1094+629A=
NM_001066.2:c.1105+629A=	NP_001057.1:n.1105+629A=
XM_011542060.1:c.1171+228A=	XP_011540362.1:n.1171+228A=
XM_011542061.1:c.1171+228A=	XP_011540363.1:n.1171+228A=
XM_011542062.1:c.1150+228A=	XP_011540364.1:n.1150+228A=
XM_011542063.1:c.1105+629A=	XP_011540365.1:n.1105+629A=
XM_011542060.2:c.1171+228A=	XP_011540362.1:n.1171+228A=
XM_011542063.2:c.1105+629A=	XP_011540365.1:n.1105+629A=
XM_017002214.1:c.586+228A=	XP_016857703.1:n.586+228A=
XM_017002215.1:c.520+629A=	XP_016857704.1:n.520+629A=
NM_001066.3:c.1105+629A= MANE Select	NP_001057.1:n.1105+629A=