Canonical Allele Identifier: CA1173064284

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258879A= , CM000663.2:g.67258879A=	GRCh38
NC_000001.10:g.67724562A= , CM000663.1:g.67724562A=	GRCh37
NC_000001.9:g.67497150A=	NCBI36
NG_011498.1:g.97394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1480A=	ENSP00000513138.1:n.1480A=
ENST00000697150.1:c.1538A=	ENSP00000513139.1:n.1538A=
ENST00000697151.1:c.1471A=	ENSP00000513140.1:n.1471A=
ENST00000697164.1:c.1551A=	ENSP00000513153.1:p.Gly517=
ENST00000697165.1:c.1338A=	ENSP00000513154.1:p.Gly446=
ENST00000347310.10:c.1641A= MANE Select	ENSP00000321345.5:p.Gly547=
ENST00000637002.1:c.1032A=	ENSP00000490340.1:p.Gly344=
ENST00000347310.9:c.1641A=	ENSP00000321345.5:p.Gly547=
ENST00000395227.2:c.435A=	ENSP00000378652.2:p.Gly145=
ENST00000425614.3:c.876A=	ENSP00000387640.2:p.Gly292=
ENST00000473881.2:c.*467A=	ENSP00000486667.1:n.*467A=
NM_144701.2:c.1641A=	NP_653302.2:p.Gly547=
XM_005270516.2:c.879A=	XP_005270573.1:p.Gly293=
XM_011540789.1:c.1731A=	XP_011539091.1:p.Gly577=
XM_011540790.1:c.1641A=	XP_011539092.1:p.Gly547=
XM_011540791.1:c.1641A=	XP_011539093.1:p.Gly547=
XM_011540790.3:c.1641A=	XP_011539092.1:p.Gly547=
XM_011540791.3:c.1641A=	XP_011539093.1:p.Gly547=
XR_001736993.1:n.1721A=
NM_144701.3:c.1641A= MANE Select	NP_653302.2:p.Gly547=