Canonical Allele Identifier: CA1173064265

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258794G= , CM000663.2:g.67258794G=	GRCh38
NC_000001.10:g.67724477G= , CM000663.1:g.67724477G=	GRCh37
NC_000001.9:g.67497065G=	NCBI36
NG_011498.1:g.97309G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1395G=	ENSP00000513138.1:n.1395G=
ENST00000697150.1:c.1453G=	ENSP00000513139.1:n.1453G=
ENST00000697151.1:c.1386G=	ENSP00000513140.1:n.1386G=
ENST00000697164.1:c.1466G=	ENSP00000513153.1:p.Gly489=
ENST00000697165.1:c.1253G=	ENSP00000513154.1:p.Gly418=
ENST00000347310.10:c.1556G= MANE Select	ENSP00000321345.5:p.Gly519=
ENST00000637002.1:c.947G=	ENSP00000490340.1:p.Gly316=
ENST00000347310.9:c.1556G=	ENSP00000321345.5:p.Gly519=
ENST00000395227.2:c.350G=	ENSP00000378652.2:p.Gly117=
ENST00000425614.3:c.791G=	ENSP00000387640.2:p.Gly264=
ENST00000473881.2:c.*382G=	ENSP00000486667.1:n.*382G=
NM_144701.2:c.1556G=	NP_653302.2:p.Gly519=
XM_005270516.2:c.794G=	XP_005270573.1:p.Gly265=
XM_011540789.1:c.1646G=	XP_011539091.1:p.Gly549=
XM_011540790.1:c.1556G=	XP_011539092.1:p.Gly519=
XM_011540791.1:c.1556G=	XP_011539093.1:p.Gly519=
XM_011540790.3:c.1556G=	XP_011539092.1:p.Gly519=
XM_011540791.3:c.1556G=	XP_011539093.1:p.Gly519=
XR_001736993.1:n.1636G=
NM_144701.3:c.1556G= MANE Select	NP_653302.2:p.Gly519=