Canonical Allele Identifier: CA1143658492

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259102A= , CM000663.2:g.67259102A=	GRCh38
NC_000001.10:g.67724785A= , CM000663.1:g.67724785A=	GRCh37
NC_000001.9:g.67497373A=	NCBI36
NG_011498.1:g.97617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1703A=	ENSP00000513138.1:n.1703A=
ENST00000697150.1:c.1761A=	ENSP00000513139.1:n.1761A=
ENST00000697151.1:c.1694A=	ENSP00000513140.1:n.1694A=
ENST00000697164.1:c.1774A=	ENSP00000513153.1:p.Asn592=
ENST00000697165.1:c.1561A=	ENSP00000513154.1:p.Asn521=
ENST00000347310.10:c.1864A= MANE Select	ENSP00000321345.5:p.Asn622=
ENST00000637002.1:c.1255A=	ENSP00000490340.1:p.Asn419=
ENST00000347310.9:c.1864A=	ENSP00000321345.5:p.Asn622=
ENST00000395227.2:c.658A=	ENSP00000378652.2:p.Asn220=
ENST00000425614.3:c.1099A=	ENSP00000387640.2:p.Asn367=
ENST00000473881.2:c.*690A=	ENSP00000486667.1:n.*690A=
NM_144701.2:c.1864A=	NP_653302.2:p.Asn622=
XM_005270516.2:c.1102A=	XP_005270573.1:p.Asn368=
XM_011540789.1:c.1954A=	XP_011539091.1:p.Asn652=
XM_011540790.1:c.1864A=	XP_011539092.1:p.Asn622=
XM_011540791.1:c.1864A=	XP_011539093.1:p.Asn622=
XM_011540790.3:c.1864A=	XP_011539092.1:p.Asn622=
XM_011540791.3:c.1864A=	XP_011539093.1:p.Asn622=
XR_001736993.1:n.1944A=
NM_144701.3:c.1864A= MANE Select	NP_653302.2:p.Asn622=