Canonical Allele Identifier: CA1173064245

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258727C= , CM000663.2:g.67258727C=	GRCh38
NC_000001.10:g.67724410C= , CM000663.1:g.67724410C=	GRCh37
NC_000001.9:g.67496998C=	NCBI36
NG_011498.1:g.97242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1328C=	ENSP00000513138.1:n.1328C=
ENST00000697150.1:c.1386C=	ENSP00000513139.1:n.1386C=
ENST00000697151.1:c.1319C=	ENSP00000513140.1:n.1319C=
ENST00000697164.1:c.1399C=	ENSP00000513153.1:p.His467=
ENST00000697165.1:c.1186C=	ENSP00000513154.1:p.His396=
ENST00000347310.10:c.1489C= MANE Select	ENSP00000321345.5:p.His497=
ENST00000637002.1:c.880C=	ENSP00000490340.1:p.His294=
ENST00000347310.9:c.1489C=	ENSP00000321345.5:p.His497=
ENST00000395227.2:c.283C=	ENSP00000378652.2:p.His95=
ENST00000425614.3:c.724C=	ENSP00000387640.2:p.His242=
ENST00000473881.2:c.*315C=	ENSP00000486667.1:n.*315C=
NM_144701.2:c.1489C=	NP_653302.2:p.His497=
XM_005270516.2:c.727C=	XP_005270573.1:p.His243=
XM_011540789.1:c.1579C=	XP_011539091.1:p.His527=
XM_011540790.1:c.1489C=	XP_011539092.1:p.His497=
XM_011540791.1:c.1489C=	XP_011539093.1:p.His497=
XM_011540790.3:c.1489C=	XP_011539092.1:p.His497=
XM_011540791.3:c.1489C=	XP_011539093.1:p.His497=
XR_001736993.1:n.1569C=
NM_144701.3:c.1489C= MANE Select	NP_653302.2:p.His497=