Canonical Allele Identifier: CA1141369968

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258927A= , CM000663.2:g.67258927A=	GRCh38
NC_000001.10:g.67724610A= , CM000663.1:g.67724610A=	GRCh37
NC_000001.9:g.67497198A=	NCBI36
NG_011498.1:g.97442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1528A=	ENSP00000513138.1:n.1528A=
ENST00000697150.1:c.1586A=	ENSP00000513139.1:n.1586A=
ENST00000697151.1:c.1519A=	ENSP00000513140.1:n.1519A=
ENST00000697164.1:c.1599A=	ENSP00000513153.1:p.Ile533=
ENST00000697165.1:c.1386A=	ENSP00000513154.1:p.Ile462=
ENST00000347310.10:c.1689A= MANE Select	ENSP00000321345.5:p.Ile563=
ENST00000637002.1:c.1080A=	ENSP00000490340.1:p.Ile360=
ENST00000347310.9:c.1689A=	ENSP00000321345.5:p.Ile563=
ENST00000395227.2:c.483A=	ENSP00000378652.2:p.Ile161=
ENST00000425614.3:c.924A=	ENSP00000387640.2:p.Ile308=
ENST00000473881.2:c.*515A=	ENSP00000486667.1:n.*515A=
NM_144701.2:c.1689A=	NP_653302.2:p.Ile563=
XM_005270516.2:c.927A=	XP_005270573.1:p.Ile309=
XM_011540789.1:c.1779A=	XP_011539091.1:p.Ile593=
XM_011540790.1:c.1689A=	XP_011539092.1:p.Ile563=
XM_011540791.1:c.1689A=	XP_011539093.1:p.Ile563=
XM_011540790.3:c.1689A=	XP_011539092.1:p.Ile563=
XM_011540791.3:c.1689A=	XP_011539093.1:p.Ile563=
XR_001736993.1:n.1769A=
NM_144701.3:c.1689A= MANE Select	NP_653302.2:p.Ile563=