Canonical Allele Identifier: CA1173064350

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259103A= , CM000663.2:g.67259103A=	GRCh38
NC_000001.10:g.67724786A= , CM000663.1:g.67724786A=	GRCh37
NC_000001.9:g.67497374A=	NCBI36
NG_011498.1:g.97618A=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1865A= MANE Select	NP_653302.2:p.Asn622=
ENST00000347310.10:c.1865A= MANE Select	ENSP00000321345.5:p.Asn622=
NM_144701.2:c.1865A=	NP_653302.2:p.Asn622=
ENST00000347310.9:c.1865A=	ENSP00000321345.5:p.Asn622=
ENST00000395227.2:c.659A=	ENSP00000378652.2:p.Asn220=
ENST00000425614.3:c.1100A=	ENSP00000387640.2:p.Asn367=
ENST00000473881.2:c.*691A=	ENSP00000486667.1:n.*691A=
ENST00000637002.1:c.1256A=	ENSP00000490340.1:p.Asn419=
ENST00000697149.1:c.1704A=	ENSP00000513138.1:n.1704A=
ENST00000697150.1:c.1762A=	ENSP00000513139.1:n.1762A=
ENST00000697151.1:c.1695A=	ENSP00000513140.1:n.1695A=
ENST00000697164.1:c.1775A=	ENSP00000513153.1:p.Asn592=
ENST00000697165.1:c.1562A=	ENSP00000513154.1:p.Asn521=
XM_005270516.2:c.1103A=	XP_005270573.1:p.Asn368=
XM_011540789.1:c.1955A=	XP_011539091.1:p.Asn652=
XM_011540790.1:c.1865A=	XP_011539092.1:p.Asn622=
XM_011540790.3:c.1865A=	XP_011539092.1:p.Asn622=
XM_011540791.1:c.1865A=	XP_011539093.1:p.Asn622=
XM_011540791.3:c.1865A=	XP_011539093.1:p.Asn622=
XR_001736993.1:n.1945A=