Canonical Allele Identifier: CA1173064342

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259071T= , CM000663.2:g.67259071T=	GRCh38
NC_000001.10:g.67724754T= , CM000663.1:g.67724754T=	GRCh37
NC_000001.9:g.67497342T=	NCBI36
NG_011498.1:g.97586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1672T=	ENSP00000513138.1:n.1672T=
ENST00000697150.1:c.1730T=	ENSP00000513139.1:n.1730T=
ENST00000697151.1:c.1663T=	ENSP00000513140.1:n.1663T=
ENST00000697164.1:c.1743T=	ENSP00000513153.1:p.Tyr581=
ENST00000697165.1:c.1530T=	ENSP00000513154.1:p.Tyr510=
ENST00000347310.10:c.1833T= MANE Select	ENSP00000321345.5:p.Tyr611=
ENST00000637002.1:c.1224T=	ENSP00000490340.1:p.Tyr408=
ENST00000347310.9:c.1833T=	ENSP00000321345.5:p.Tyr611=
ENST00000395227.2:c.627T=	ENSP00000378652.2:p.Tyr209=
ENST00000425614.3:c.1068T=	ENSP00000387640.2:p.Tyr356=
ENST00000473881.2:c.*659T=	ENSP00000486667.1:n.*659T=
NM_144701.2:c.1833T=	NP_653302.2:p.Tyr611=
XM_005270516.2:c.1071T=	XP_005270573.1:p.Tyr357=
XM_011540789.1:c.1923T=	XP_011539091.1:p.Tyr641=
XM_011540790.1:c.1833T=	XP_011539092.1:p.Tyr611=
XM_011540791.1:c.1833T=	XP_011539093.1:p.Tyr611=
XM_011540790.3:c.1833T=	XP_011539092.1:p.Tyr611=
XM_011540791.3:c.1833T=	XP_011539093.1:p.Tyr611=
XR_001736993.1:n.1913T=
NM_144701.3:c.1833T= MANE Select	NP_653302.2:p.Tyr611=