Canonical Allele Identifier: CA340725744

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705868G>T (hg19) ; chr1:g.67240185G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240185G>T , CM000663.2:g.67240185G>T	GRCh38
NC_000001.10:g.67705868G>T , CM000663.1:g.67705868G>T	GRCh37
NC_000001.9:g.67478456G>T	NCBI36
NG_011498.1:g.78700G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.928G>T	ENSP00000513137.1:n.928G>T
ENST00000697149.1:c.891G>T	ENSP00000513138.1:n.891G>T
ENST00000697150.1:c.1045+3383G>T	ENSP00000513139.1:n.1045+3383G>T
ENST00000697151.1:c.1045+3383G>T	ENSP00000513140.1:n.1045+3383G>T
ENST00000697152.1:c.799-15652G>T	ENSP00000513141.1:n.799-15652G>T
ENST00000697153.1:c.795-15652G>T	ENSP00000513142.1:n.795-15652G>T
ENST00000697154.1:c.956-18293G>T	ENSP00000513143.1:n.956-18293G>T
ENST00000697155.1:c.649-18293G>T	ENSP00000513144.1:n.649-18293G>T
ENST00000697156.1:c.1052G>T	ENSP00000513145.1:p.Arg351Ile
ENST00000697157.1:c.906G>T	ENSP00000513146.1:n.906G>T
ENST00000697158.1:c.895G>T	ENSP00000513147.1:n.895G>T
ENST00000697159.1:c.745G>T	ENSP00000513148.1:n.745G>T
ENST00000697160.1:c.956-15652G>T	ENSP00000513149.1:n.956-15652G>T
ENST00000697161.1:c.588G>T	ENSP00000513150.1:n.588G>T
ENST00000697162.1:c.981G>T	ENSP00000513151.1:n.981G>T
ENST00000697163.1:c.1052G>T	ENSP00000513152.1:p.Arg351Ile
ENST00000697164.1:c.962G>T	ENSP00000513153.1:p.Arg321Ile
ENST00000697165.1:c.749G>T	ENSP00000513154.1:p.Arg250Ile
ENST00000697223.1:c.801G>T	ENSP00000513190.1:n.801G>T
ENST00000697224.1:c.884+3383G>T	ENSP00000513191.1:n.884+3383G>T
ENST00000697225.1:c.655G>T	ENSP00000513192.1:n.655G>T
ENST00000697226.1:c.738+3383G>T	ENSP00000513193.1:n.738+3383G>T
ENST00000697227.1:c.888G>T	ENSP00000513194.1:n.888G>T
ENST00000697228.1:c.744G>T	ENSP00000513195.1:n.744G>T
ENST00000697229.1:c.885-15652G>T	ENSP00000513196.1:n.885-15652G>T
ENST00000697230.1:c.962G>T	ENSP00000513197.1:p.Arg321Ile
ENST00000697231.1:c.957G>T	ENSP00000513198.1:n.957G>T
ENST00000697232.1:c.981G>T	ENSP00000513199.1:n.981G>T
ENST00000347310.10:c.1052G>T MANE Select	ENSP00000321345.5:p.Arg351Ile
ENST00000637002.1:c.443G>T	ENSP00000490340.1:p.Arg148Ile
ENST00000347310.9:c.1052G>T	ENSP00000321345.5:p.Arg351Ile
ENST00000395227.2:c.-58-15652G>T	ENSP00000378652.2:n.-58-15652G>T
ENST00000425614.3:c.287G>T	ENSP00000387640.2:p.Arg96Ile
ENST00000473881.2:c.191-15652G>T	ENSP00000486667.1:n.191-15652G>T
NM_144701.2:c.1052G>T	NP_653302.2:p.Arg351Ile
XM_005270516.2:c.290G>T	XP_005270573.1:p.Arg97Ile
XM_011540789.1:c.1142G>T	XP_011539091.1:p.Arg381Ile
XM_011540790.1:c.1052G>T	XP_011539092.1:p.Arg351Ile
XM_011540791.1:c.1052G>T	XP_011539093.1:p.Arg351Ile
XM_011540790.3:c.1052G>T	XP_011539092.1:p.Arg351Ile
XM_011540791.3:c.1052G>T	XP_011539093.1:p.Arg351Ile
XR_001736993.1:n.1228+3383G>T
NM_144701.3:c.1052G>T MANE Select	NP_653302.2:p.Arg351Ile