Canonical Allele Identifier: CA1173064283

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258877G= , CM000663.2:g.67258877G=	GRCh38
NC_000001.10:g.67724560G= , CM000663.1:g.67724560G=	GRCh37
NC_000001.9:g.67497148G=	NCBI36
NG_011498.1:g.97392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1478G=	ENSP00000513138.1:n.1478G=
ENST00000697150.1:c.1536G=	ENSP00000513139.1:n.1536G=
ENST00000697151.1:c.1469G=	ENSP00000513140.1:n.1469G=
ENST00000697164.1:c.1549G=	ENSP00000513153.1:p.Gly517=
ENST00000697165.1:c.1336G=	ENSP00000513154.1:p.Gly446=
ENST00000347310.10:c.1639G= MANE Select	ENSP00000321345.5:p.Gly547=
ENST00000637002.1:c.1030G=	ENSP00000490340.1:p.Gly344=
ENST00000347310.9:c.1639G=	ENSP00000321345.5:p.Gly547=
ENST00000395227.2:c.433G=	ENSP00000378652.2:p.Gly145=
ENST00000425614.3:c.874G=	ENSP00000387640.2:p.Gly292=
ENST00000473881.2:c.*465G=	ENSP00000486667.1:n.*465G=
NM_144701.2:c.1639G=	NP_653302.2:p.Gly547=
XM_005270516.2:c.877G=	XP_005270573.1:p.Gly293=
XM_011540789.1:c.1729G=	XP_011539091.1:p.Gly577=
XM_011540790.1:c.1639G=	XP_011539092.1:p.Gly547=
XM_011540791.1:c.1639G=	XP_011539093.1:p.Gly547=
XM_011540790.3:c.1639G=	XP_011539092.1:p.Gly547=
XM_011540791.3:c.1639G=	XP_011539093.1:p.Gly547=
XR_001736993.1:n.1719G=
NM_144701.3:c.1639G= MANE Select	NP_653302.2:p.Gly547=