Canonical Allele Identifier: CA1173064302

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258937G= , CM000663.2:g.67258937G=	GRCh38
NC_000001.10:g.67724620G= , CM000663.1:g.67724620G=	GRCh37
NC_000001.9:g.67497208G=	NCBI36
NG_011498.1:g.97452G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1538G=	ENSP00000513138.1:n.1538G=
ENST00000697150.1:c.1596G=	ENSP00000513139.1:n.1596G=
ENST00000697151.1:c.1529G=	ENSP00000513140.1:n.1529G=
ENST00000697164.1:c.1609G=	ENSP00000513153.1:p.Val537=
ENST00000697165.1:c.1396G=	ENSP00000513154.1:p.Val466=
ENST00000347310.10:c.1699G= MANE Select	ENSP00000321345.5:p.Val567=
ENST00000637002.1:c.1090G=	ENSP00000490340.1:p.Val364=
ENST00000347310.9:c.1699G=	ENSP00000321345.5:p.Val567=
ENST00000395227.2:c.493G=	ENSP00000378652.2:p.Val165=
ENST00000425614.3:c.934G=	ENSP00000387640.2:p.Val312=
ENST00000473881.2:c.*525G=	ENSP00000486667.1:n.*525G=
NM_144701.2:c.1699G=	NP_653302.2:p.Val567=
XM_005270516.2:c.937G=	XP_005270573.1:p.Val313=
XM_011540789.1:c.1789G=	XP_011539091.1:p.Val597=
XM_011540790.1:c.1699G=	XP_011539092.1:p.Val567=
XM_011540791.1:c.1699G=	XP_011539093.1:p.Val567=
XM_011540790.3:c.1699G=	XP_011539092.1:p.Val567=
XM_011540791.3:c.1699G=	XP_011539093.1:p.Val567=
XR_001736993.1:n.1779G=
NM_144701.3:c.1699G= MANE Select	NP_653302.2:p.Val567=