Canonical Allele Identifier: CA3081745106

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259063A= , CM000663.2:g.67259063A=	GRCh38
NC_000001.10:g.67724746A= , CM000663.1:g.67724746A=	GRCh37
NC_000001.9:g.67497334A=	NCBI36
NG_011498.1:g.97578A=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1825A= MANE Select	NP_653302.2:p.Asn609=
ENST00000347310.10:c.1825A= MANE Select	ENSP00000321345.5:p.Asn609=
NM_144701.2:c.1825A=	NP_653302.2:p.Asn609=
ENST00000347310.9:c.1825A=	ENSP00000321345.5:p.Asn609=
ENST00000395227.2:c.619A=	ENSP00000378652.2:p.Asn207=
ENST00000425614.3:c.1060A=	ENSP00000387640.2:p.Asn354=
ENST00000473881.2:c.*651A=	ENSP00000486667.1:n.*651A=
ENST00000637002.1:c.1216A=	ENSP00000490340.1:p.Asn406=
ENST00000697149.1:c.1664A=	ENSP00000513138.1:n.1664A=
ENST00000697150.1:c.1722A=	ENSP00000513139.1:n.1722A=
ENST00000697151.1:c.1655A=	ENSP00000513140.1:n.1655A=
ENST00000697164.1:c.1735A=	ENSP00000513153.1:p.Asn579=
ENST00000697165.1:c.1522A=	ENSP00000513154.1:p.Asn508=
XM_005270516.2:c.1063A=	XP_005270573.1:p.Asn355=
XM_011540789.1:c.1915A=	XP_011539091.1:p.Asn639=
XM_011540790.1:c.1825A=	XP_011539092.1:p.Asn609=
XM_011540790.3:c.1825A=	XP_011539092.1:p.Asn609=
XM_011540791.1:c.1825A=	XP_011539093.1:p.Asn609=
XM_011540791.3:c.1825A=	XP_011539093.1:p.Asn609=
XR_001736993.1:n.1905A=