Canonical Allele Identifier: CA340725948

Gene: IL23R

Linked Data

• dbSNP Id: rs1168522773
• gnomAD v2: 1-67705963-G-A
• gnomAD v4: 1-67240280-G-A
• MyVariant Identifiers: chr1:g.67705963G>A (hg19) ; chr1:g.67240280G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240280G>A , CM000663.2:g.67240280G>A	GRCh38
NC_000001.10:g.67705963G>A , CM000663.1:g.67705963G>A	GRCh37
NC_000001.9:g.67478551G>A	NCBI36
NG_011498.1:g.78795G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.1023G>A	ENSP00000513137.1:n.1023G>A
ENST00000697149.1:c.986G>A	ENSP00000513138.1:n.986G>A
ENST00000697150.1:c.1045+3478G>A	ENSP00000513139.1:n.1045+3478G>A
ENST00000697151.1:c.1045+3478G>A	ENSP00000513140.1:n.1045+3478G>A
ENST00000697152.1:c.799-15557G>A	ENSP00000513141.1:n.799-15557G>A
ENST00000697153.1:c.795-15557G>A	ENSP00000513142.1:n.795-15557G>A
ENST00000697154.1:c.956-18198G>A	ENSP00000513143.1:n.956-18198G>A
ENST00000697155.1:c.649-18198G>A	ENSP00000513144.1:n.649-18198G>A
ENST00000697156.1:c.1147G>A	ENSP00000513145.1:p.Gly383Arg
ENST00000697157.1:c.1001G>A	ENSP00000513146.1:n.1001G>A
ENST00000697158.1:c.990G>A	ENSP00000513147.1:n.990G>A
ENST00000697159.1:c.840G>A	ENSP00000513148.1:n.840G>A
ENST00000697160.1:c.956-15557G>A	ENSP00000513149.1:n.956-15557G>A
ENST00000697161.1:c.683G>A	ENSP00000513150.1:n.683G>A
ENST00000697162.1:c.1076G>A	ENSP00000513151.1:n.1076G>A
ENST00000697163.1:c.1147G>A	ENSP00000513152.1:p.Gly383Arg
ENST00000697164.1:c.1057G>A	ENSP00000513153.1:p.Gly353Arg
ENST00000697165.1:c.844G>A	ENSP00000513154.1:p.Gly282Arg
ENST00000697223.1:c.896G>A	ENSP00000513190.1:n.896G>A
ENST00000697224.1:c.884+3478G>A	ENSP00000513191.1:n.884+3478G>A
ENST00000697225.1:c.750G>A	ENSP00000513192.1:n.750G>A
ENST00000697226.1:c.738+3478G>A	ENSP00000513193.1:n.738+3478G>A
ENST00000697227.1:c.983G>A	ENSP00000513194.1:n.983G>A
ENST00000697228.1:c.839G>A	ENSP00000513195.1:n.839G>A
ENST00000697229.1:c.885-15557G>A	ENSP00000513196.1:n.885-15557G>A
ENST00000697230.1:c.1057G>A	ENSP00000513197.1:p.Gly353Arg
ENST00000697231.1:c.1052G>A	ENSP00000513198.1:n.1052G>A
ENST00000697232.1:c.1076G>A	ENSP00000513199.1:n.1076G>A
ENST00000347310.10:c.1147G>A MANE Select	ENSP00000321345.5:p.Gly383Arg
ENST00000637002.1:c.538G>A	ENSP00000490340.1:p.Gly180Arg
ENST00000347310.9:c.1147G>A	ENSP00000321345.5:p.Gly383Arg
ENST00000395227.2:c.-58-15557G>A	ENSP00000378652.2:n.-58-15557G>A
ENST00000425614.3:c.382G>A	ENSP00000387640.2:p.Gly128Arg
ENST00000473881.2:c.191-15557G>A	ENSP00000486667.1:n.191-15557G>A
NM_144701.2:c.1147G>A	NP_653302.2:p.Gly383Arg
XM_005270516.2:c.385G>A	XP_005270573.1:p.Gly129Arg
XM_011540789.1:c.1237G>A	XP_011539091.1:p.Gly413Arg
XM_011540790.1:c.1147G>A	XP_011539092.1:p.Gly383Arg
XM_011540791.1:c.1147G>A	XP_011539093.1:p.Gly383Arg
XM_011540790.3:c.1147G>A	XP_011539092.1:p.Gly383Arg
XM_011540791.3:c.1147G>A	XP_011539093.1:p.Gly383Arg
XR_001736993.1:n.1228+3478G>A
NM_144701.3:c.1147G>A MANE Select	NP_653302.2:p.Gly383Arg