Canonical Allele Identifier: CA1173064333

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259039G= , CM000663.2:g.67259039G=	GRCh38
NC_000001.10:g.67724722G= , CM000663.1:g.67724722G=	GRCh37
NC_000001.9:g.67497310G=	NCBI36
NG_011498.1:g.97554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1640G=	ENSP00000513138.1:n.1640G=
ENST00000697150.1:c.1698G=	ENSP00000513139.1:n.1698G=
ENST00000697151.1:c.1631G=	ENSP00000513140.1:n.1631G=
ENST00000697164.1:c.1711G=	ENSP00000513153.1:p.Val571=
ENST00000697165.1:c.1498G=	ENSP00000513154.1:p.Val500=
ENST00000347310.10:c.1801G= MANE Select	ENSP00000321345.5:p.Val601=
ENST00000637002.1:c.1192G=	ENSP00000490340.1:p.Val398=
ENST00000347310.9:c.1801G=	ENSP00000321345.5:p.Val601=
ENST00000395227.2:c.595G=	ENSP00000378652.2:p.Val199=
ENST00000425614.3:c.1036G=	ENSP00000387640.2:p.Val346=
ENST00000473881.2:c.*627G=	ENSP00000486667.1:n.*627G=
NM_144701.2:c.1801G=	NP_653302.2:p.Val601=
XM_005270516.2:c.1039G=	XP_005270573.1:p.Val347=
XM_011540789.1:c.1891G=	XP_011539091.1:p.Val631=
XM_011540790.1:c.1801G=	XP_011539092.1:p.Val601=
XM_011540791.1:c.1801G=	XP_011539093.1:p.Val601=
XM_011540790.3:c.1801G=	XP_011539092.1:p.Val601=
XM_011540791.3:c.1801G=	XP_011539093.1:p.Val601=
XR_001736993.1:n.1881G=
NM_144701.3:c.1801G= MANE Select	NP_653302.2:p.Val601=