Canonical Allele Identifier: CA1173064269

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258818A= , CM000663.2:g.67258818A=	GRCh38
NC_000001.10:g.67724501A= , CM000663.1:g.67724501A=	GRCh37
NC_000001.9:g.67497089A=	NCBI36
NG_011498.1:g.97333A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1419A=	ENSP00000513138.1:n.1419A=
ENST00000697150.1:c.1477A=	ENSP00000513139.1:n.1477A=
ENST00000697151.1:c.1410A=	ENSP00000513140.1:n.1410A=
ENST00000697164.1:c.1490A=	ENSP00000513153.1:p.His497=
ENST00000697165.1:c.1277A=	ENSP00000513154.1:p.His426=
ENST00000347310.10:c.1580A= MANE Select	ENSP00000321345.5:p.His527=
ENST00000637002.1:c.971A=	ENSP00000490340.1:p.His324=
ENST00000347310.9:c.1580A=	ENSP00000321345.5:p.His527=
ENST00000395227.2:c.374A=	ENSP00000378652.2:p.His125=
ENST00000425614.3:c.815A=	ENSP00000387640.2:p.His272=
ENST00000473881.2:c.*406A=	ENSP00000486667.1:n.*406A=
NM_144701.2:c.1580A=	NP_653302.2:p.His527=
XM_005270516.2:c.818A=	XP_005270573.1:p.His273=
XM_011540789.1:c.1670A=	XP_011539091.1:p.His557=
XM_011540790.1:c.1580A=	XP_011539092.1:p.His527=
XM_011540791.1:c.1580A=	XP_011539093.1:p.His527=
XM_011540790.3:c.1580A=	XP_011539092.1:p.His527=
XM_011540791.3:c.1580A=	XP_011539093.1:p.His527=
XR_001736993.1:n.1660A=
NM_144701.3:c.1580A= MANE Select	NP_653302.2:p.His527=