Canonical Allele Identifier: CA1154001453

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192995G= , CM000663.2:g.12192995G=	GRCh38
NC_000001.10:g.12253052G= , CM000663.1:g.12253052G=	GRCh37
NC_000001.9:g.12175639G=	NCBI36
NG_029791.1:g.30993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.684G= MANE Select	ENSP00000365435.3:p.Gln228=
ENST00000376259.6:c.684G=	ENSP00000365435.3:p.Gln228=
ENST00000489921.1:n.396G=
ENST00000492361.1:n.673G=
NM_001066.2:c.684G=	NP_001057.1:p.Gln228=
XM_011542060.1:c.684G=	XP_011540362.1:p.Gln228=
XM_011542061.1:c.684G=	XP_011540363.1:p.Gln228=
XM_011542062.1:c.663G=	XP_011540364.1:p.Gln221=
XM_011542063.1:c.684G=	XP_011540365.1:p.Gln228=
XM_011542060.2:c.684G=	XP_011540362.1:p.Gln228=
XM_011542063.2:c.684G=	XP_011540365.1:p.Gln228=
XM_017002211.1:c.684G=	XP_016857700.1:p.Gln228=
XM_017002214.1:c.99G=	XP_016857703.1:p.Gln33=
XM_017002215.1:c.99G=	XP_016857704.1:p.Gln33=
NM_001066.3:c.684G= MANE Select	NP_001057.1:p.Gln228=