Canonical Allele Identifier: CA1148441934

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259094G= , CM000663.2:g.67259094G=	GRCh38
NC_000001.10:g.67724777G= , CM000663.1:g.67724777G=	GRCh37
NC_000001.9:g.67497365G=	NCBI36
NG_011498.1:g.97609G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1695G=	ENSP00000513138.1:n.1695G=
ENST00000697150.1:c.1753G=	ENSP00000513139.1:n.1753G=
ENST00000697151.1:c.1686G=	ENSP00000513140.1:n.1686G=
ENST00000697164.1:c.1766G=	ENSP00000513153.1:p.Ser589=
ENST00000697165.1:c.1553G=	ENSP00000513154.1:p.Ser518=
ENST00000347310.10:c.1856G= MANE Select	ENSP00000321345.5:p.Ser619=
ENST00000637002.1:c.1247G=	ENSP00000490340.1:p.Ser416=
ENST00000347310.9:c.1856G=	ENSP00000321345.5:p.Ser619=
ENST00000395227.2:c.650G=	ENSP00000378652.2:p.Ser217=
ENST00000425614.3:c.1091G=	ENSP00000387640.2:p.Ser364=
ENST00000473881.2:c.*682G=	ENSP00000486667.1:n.*682G=
NM_144701.2:c.1856G=	NP_653302.2:p.Ser619=
XM_005270516.2:c.1094G=	XP_005270573.1:p.Ser365=
XM_011540789.1:c.1946G=	XP_011539091.1:p.Ser649=
XM_011540790.1:c.1856G=	XP_011539092.1:p.Ser619=
XM_011540791.1:c.1856G=	XP_011539093.1:p.Ser619=
XM_011540790.3:c.1856G=	XP_011539092.1:p.Ser619=
XM_011540791.3:c.1856G=	XP_011539093.1:p.Ser619=
XR_001736993.1:n.1936G=
NM_144701.3:c.1856G= MANE Select	NP_653302.2:p.Ser619=