Canonical Allele Identifier: CA1173064351

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259107G= , CM000663.2:g.67259107G=	GRCh38
NC_000001.10:g.67724790G= , CM000663.1:g.67724790G=	GRCh37
NC_000001.9:g.67497378G=	NCBI36
NG_011498.1:g.97622G=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1869G= MANE Select	NP_653302.2:p.Arg623=
ENST00000347310.10:c.1869G= MANE Select	ENSP00000321345.5:p.Arg623=
NM_144701.2:c.1869G=	NP_653302.2:p.Arg623=
ENST00000347310.9:c.1869G=	ENSP00000321345.5:p.Arg623=
ENST00000395227.2:c.663G=	ENSP00000378652.2:p.Arg221=
ENST00000425614.3:c.1104G=	ENSP00000387640.2:p.Arg368=
ENST00000473881.2:c.*695G=	ENSP00000486667.1:n.*695G=
ENST00000637002.1:c.1260G=	ENSP00000490340.1:p.Arg420=
ENST00000697149.1:c.1708G=	ENSP00000513138.1:n.1708G=
ENST00000697150.1:c.1766G=	ENSP00000513139.1:n.1766G=
ENST00000697151.1:c.1699G=	ENSP00000513140.1:n.1699G=
ENST00000697164.1:c.1779G=	ENSP00000513153.1:p.Arg593=
ENST00000697165.1:c.1566G=	ENSP00000513154.1:p.Arg522=
XM_005270516.2:c.1107G=	XP_005270573.1:p.Arg369=
XM_011540789.1:c.1959G=	XP_011539091.1:p.Arg653=
XM_011540790.1:c.1869G=	XP_011539092.1:p.Arg623=
XM_011540790.3:c.1869G=	XP_011539092.1:p.Arg623=
XM_011540791.1:c.1869G=	XP_011539093.1:p.Arg623=
XM_011540791.3:c.1869G=	XP_011539093.1:p.Arg623=
XR_001736993.1:n.1949G=