Canonical Allele Identifier: CA1173064305

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258946G= , CM000663.2:g.67258946G=	GRCh38
NC_000001.10:g.67724629G= , CM000663.1:g.67724629G=	GRCh37
NC_000001.9:g.67497217G=	NCBI36
NG_011498.1:g.97461G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1547G=	ENSP00000513138.1:n.1547G=
ENST00000697150.1:c.1605G=	ENSP00000513139.1:n.1605G=
ENST00000697151.1:c.1538G=	ENSP00000513140.1:n.1538G=
ENST00000697164.1:c.1618G=	ENSP00000513153.1:p.Glu540=
ENST00000697165.1:c.1405G=	ENSP00000513154.1:p.Glu469=
ENST00000347310.10:c.1708G= MANE Select	ENSP00000321345.5:p.Glu570=
ENST00000637002.1:c.1099G=	ENSP00000490340.1:p.Glu367=
ENST00000347310.9:c.1708G=	ENSP00000321345.5:p.Glu570=
ENST00000395227.2:c.502G=	ENSP00000378652.2:p.Glu168=
ENST00000425614.3:c.943G=	ENSP00000387640.2:p.Glu315=
ENST00000473881.2:c.*534G=	ENSP00000486667.1:n.*534G=
NM_144701.2:c.1708G=	NP_653302.2:p.Glu570=
XM_005270516.2:c.946G=	XP_005270573.1:p.Glu316=
XM_011540789.1:c.1798G=	XP_011539091.1:p.Glu600=
XM_011540790.1:c.1708G=	XP_011539092.1:p.Glu570=
XM_011540791.1:c.1708G=	XP_011539093.1:p.Glu570=
XM_011540790.3:c.1708G=	XP_011539092.1:p.Glu570=
XM_011540791.3:c.1708G=	XP_011539093.1:p.Glu570=
XR_001736993.1:n.1788G=
NM_144701.3:c.1708G= MANE Select	NP_653302.2:p.Glu570=