Canonical Allele Identifier: CA3073738743

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259119G= , CM000663.2:g.67259119G=	GRCh38
NC_000001.10:g.67724802G= , CM000663.1:g.67724802G=	GRCh37
NC_000001.9:g.67497390G=	NCBI36
NG_011498.1:g.97634G=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1881G= MANE Select	NP_653302.2:p.Leu627=
ENST00000347310.10:c.1881G= MANE Select	ENSP00000321345.5:p.Leu627=
NM_144701.2:c.1881G=	NP_653302.2:p.Leu627=
ENST00000347310.9:c.1881G=	ENSP00000321345.5:p.Leu627=
ENST00000395227.2:c.675G=	ENSP00000378652.2:p.Leu225=
ENST00000425614.3:c.1116G=	ENSP00000387640.2:p.Leu372=
ENST00000473881.2:c.*707G=	ENSP00000486667.1:n.*707G=
ENST00000637002.1:c.1272G=	ENSP00000490340.1:p.Leu424=
ENST00000697149.1:c.1720G=	ENSP00000513138.1:n.1720G=
ENST00000697150.1:c.1778G=	ENSP00000513139.1:n.1778G=
ENST00000697151.1:c.1711G=	ENSP00000513140.1:n.1711G=
ENST00000697164.1:c.1791G=	ENSP00000513153.1:p.Leu597=
ENST00000697165.1:c.1578G=	ENSP00000513154.1:p.Leu526=
XM_005270516.2:c.1119G=	XP_005270573.1:p.Leu373=
XM_011540789.1:c.1971G=	XP_011539091.1:p.Leu657=
XM_011540790.1:c.1881G=	XP_011539092.1:p.Leu627=
XM_011540790.3:c.1881G=	XP_011539092.1:p.Leu627=
XM_011540791.1:c.1881G=	XP_011539093.1:p.Leu627=
XM_011540791.3:c.1881G=	XP_011539093.1:p.Leu627=
XR_001736993.1:n.1961G=