Canonical Allele Identifier: CA3081745088

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259055C= , CM000663.2:g.67259055C=	GRCh38
NC_000001.10:g.67724738C= , CM000663.1:g.67724738C=	GRCh37
NC_000001.9:g.67497326C=	NCBI36
NG_011498.1:g.97570C=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1817C= MANE Select	NP_653302.2:p.Pro606=
ENST00000347310.10:c.1817C= MANE Select	ENSP00000321345.5:p.Pro606=
NM_144701.2:c.1817C=	NP_653302.2:p.Pro606=
ENST00000347310.9:c.1817C=	ENSP00000321345.5:p.Pro606=
ENST00000395227.2:c.611C=	ENSP00000378652.2:p.Pro204=
ENST00000425614.3:c.1052C=	ENSP00000387640.2:p.Pro351=
ENST00000473881.2:c.*643C=	ENSP00000486667.1:n.*643C=
ENST00000637002.1:c.1208C=	ENSP00000490340.1:p.Pro403=
ENST00000697149.1:c.1656C=	ENSP00000513138.1:n.1656C=
ENST00000697150.1:c.1714C=	ENSP00000513139.1:n.1714C=
ENST00000697151.1:c.1647C=	ENSP00000513140.1:n.1647C=
ENST00000697164.1:c.1727C=	ENSP00000513153.1:p.Pro576=
ENST00000697165.1:c.1514C=	ENSP00000513154.1:p.Pro505=
XM_005270516.2:c.1055C=	XP_005270573.1:p.Pro352=
XM_011540789.1:c.1907C=	XP_011539091.1:p.Pro636=
XM_011540790.1:c.1817C=	XP_011539092.1:p.Pro606=
XM_011540790.3:c.1817C=	XP_011539092.1:p.Pro606=
XM_011540791.1:c.1817C=	XP_011539093.1:p.Pro606=
XM_011540791.3:c.1817C=	XP_011539093.1:p.Pro606=
XR_001736993.1:n.1897C=