Canonical Allele Identifier: CA1173064356

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259126T= , CM000663.2:g.67259126T=	GRCh38
NC_000001.10:g.67724809T= , CM000663.1:g.67724809T=	GRCh37
NC_000001.9:g.67497397T=	NCBI36
NG_011498.1:g.97641T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1888T= MANE Select	NP_653302.2:p.Ter630=
ENST00000347310.10:c.1888T= MANE Select	ENSP00000321345.5:p.Ter630=
NM_144701.2:c.1888T=	NP_653302.2:p.Ter630=
ENST00000347310.9:c.1888T=	ENSP00000321345.5:p.Ter630=
ENST00000395227.2:c.682T=	ENSP00000378652.2:p.Ter228=
ENST00000425614.3:c.1123T=	ENSP00000387640.2:p.Ter375=
ENST00000473881.2:c.*714T=	ENSP00000486667.1:n.*714T=
ENST00000637002.1:c.1279T=	ENSP00000490340.1:p.Ter427=
ENST00000697164.1:c.1798T=	ENSP00000513153.1:p.Ter600=
ENST00000697165.1:c.1585T=	ENSP00000513154.1:p.Ter529=
XM_005270516.2:c.1126T=	XP_005270573.1:p.Ter376=
XM_011540789.1:c.1978T=	XP_011539091.1:p.Ter660=
XM_011540790.1:c.1888T=	XP_011539092.1:p.Ter630=
XM_011540790.3:c.1888T=	XP_011539092.1:p.Ter630=
XM_011540791.1:c.1888T=	XP_011539093.1:p.Ter630=
XM_011540791.3:c.1888T=	XP_011539093.1:p.Ter630=