Canonical Allele Identifier: CA1173064276

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258849G= , CM000663.2:g.67258849G=	GRCh38
NC_000001.10:g.67724532G= , CM000663.1:g.67724532G=	GRCh37
NC_000001.9:g.67497120G=	NCBI36
NG_011498.1:g.97364G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1450G=	ENSP00000513138.1:n.1450G=
ENST00000697150.1:c.1508G=	ENSP00000513139.1:n.1508G=
ENST00000697151.1:c.1441G=	ENSP00000513140.1:n.1441G=
ENST00000697164.1:c.1521G=	ENSP00000513153.1:p.Val507=
ENST00000697165.1:c.1308G=	ENSP00000513154.1:p.Val436=
ENST00000347310.10:c.1611G= MANE Select	ENSP00000321345.5:p.Val537=
ENST00000637002.1:c.1002G=	ENSP00000490340.1:p.Val334=
ENST00000347310.9:c.1611G=	ENSP00000321345.5:p.Val537=
ENST00000395227.2:c.405G=	ENSP00000378652.2:p.Val135=
ENST00000425614.3:c.846G=	ENSP00000387640.2:p.Val282=
ENST00000473881.2:c.*437G=	ENSP00000486667.1:n.*437G=
NM_144701.2:c.1611G=	NP_653302.2:p.Val537=
XM_005270516.2:c.849G=	XP_005270573.1:p.Val283=
XM_011540789.1:c.1701G=	XP_011539091.1:p.Val567=
XM_011540790.1:c.1611G=	XP_011539092.1:p.Val537=
XM_011540791.1:c.1611G=	XP_011539093.1:p.Val537=
XM_011540790.3:c.1611G=	XP_011539092.1:p.Val537=
XM_011540791.3:c.1611G=	XP_011539093.1:p.Val537=
XR_001736993.1:n.1691G=
NM_144701.3:c.1611G= MANE Select	NP_653302.2:p.Val537=