Canonical Allele Identifier: CA3081745066

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259044T= , CM000663.2:g.67259044T=	GRCh38
NC_000001.10:g.67724727T= , CM000663.1:g.67724727T=	GRCh37
NC_000001.9:g.67497315T=	NCBI36
NG_011498.1:g.97559T=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1806T= MANE Select	NP_653302.2:p.Asn602=
ENST00000347310.10:c.1806T= MANE Select	ENSP00000321345.5:p.Asn602=
NM_144701.2:c.1806T=	NP_653302.2:p.Asn602=
ENST00000347310.9:c.1806T=	ENSP00000321345.5:p.Asn602=
ENST00000395227.2:c.600T=	ENSP00000378652.2:p.Asn200=
ENST00000425614.3:c.1041T=	ENSP00000387640.2:p.Asn347=
ENST00000473881.2:c.*632T=	ENSP00000486667.1:n.*632T=
ENST00000637002.1:c.1197T=	ENSP00000490340.1:p.Asn399=
ENST00000697149.1:c.1645T=	ENSP00000513138.1:n.1645T=
ENST00000697150.1:c.1703T=	ENSP00000513139.1:n.1703T=
ENST00000697151.1:c.1636T=	ENSP00000513140.1:n.1636T=
ENST00000697164.1:c.1716T=	ENSP00000513153.1:p.Asn572=
ENST00000697165.1:c.1503T=	ENSP00000513154.1:p.Asn501=
XM_005270516.2:c.1044T=	XP_005270573.1:p.Asn348=
XM_011540789.1:c.1896T=	XP_011539091.1:p.Asn632=
XM_011540790.1:c.1806T=	XP_011539092.1:p.Asn602=
XM_011540790.3:c.1806T=	XP_011539092.1:p.Asn602=
XM_011540791.1:c.1806T=	XP_011539093.1:p.Asn602=
XM_011540791.3:c.1806T=	XP_011539093.1:p.Asn602=
XR_001736993.1:n.1886T=