Canonical Allele Identifier: CA340725775

Gene: IL23R

Linked Data

• gnomAD v4: 1-67240199-C-G
• MyVariant Identifiers: chr1:g.67705882C>G (hg19) ; chr1:g.67240199C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240199C>G , CM000663.2:g.67240199C>G	GRCh38
NC_000001.10:g.67705882C>G , CM000663.1:g.67705882C>G	GRCh37
NC_000001.9:g.67478470C>G	NCBI36
NG_011498.1:g.78714C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.942C>G	ENSP00000513137.1:n.942C>G
ENST00000697149.1:c.905C>G	ENSP00000513138.1:n.905C>G
ENST00000697150.1:c.1045+3397C>G	ENSP00000513139.1:n.1045+3397C>G
ENST00000697151.1:c.1045+3397C>G	ENSP00000513140.1:n.1045+3397C>G
ENST00000697152.1:c.799-15638C>G	ENSP00000513141.1:n.799-15638C>G
ENST00000697153.1:c.795-15638C>G	ENSP00000513142.1:n.795-15638C>G
ENST00000697154.1:c.956-18279C>G	ENSP00000513143.1:n.956-18279C>G
ENST00000697155.1:c.649-18279C>G	ENSP00000513144.1:n.649-18279C>G
ENST00000697156.1:c.1066C>G	ENSP00000513145.1:p.Leu356Val
ENST00000697157.1:c.920C>G	ENSP00000513146.1:n.920C>G
ENST00000697158.1:c.909C>G	ENSP00000513147.1:n.909C>G
ENST00000697159.1:c.759C>G	ENSP00000513148.1:n.759C>G
ENST00000697160.1:c.956-15638C>G	ENSP00000513149.1:n.956-15638C>G
ENST00000697161.1:c.602C>G	ENSP00000513150.1:n.602C>G
ENST00000697162.1:c.995C>G	ENSP00000513151.1:n.995C>G
ENST00000697163.1:c.1066C>G	ENSP00000513152.1:p.Leu356Val
ENST00000697164.1:c.976C>G	ENSP00000513153.1:p.Leu326Val
ENST00000697165.1:c.763C>G	ENSP00000513154.1:p.Leu255Val
ENST00000697223.1:c.815C>G	ENSP00000513190.1:n.815C>G
ENST00000697224.1:c.884+3397C>G	ENSP00000513191.1:n.884+3397C>G
ENST00000697225.1:c.669C>G	ENSP00000513192.1:n.669C>G
ENST00000697226.1:c.738+3397C>G	ENSP00000513193.1:n.738+3397C>G
ENST00000697227.1:c.902C>G	ENSP00000513194.1:n.902C>G
ENST00000697228.1:c.758C>G	ENSP00000513195.1:n.758C>G
ENST00000697229.1:c.885-15638C>G	ENSP00000513196.1:n.885-15638C>G
ENST00000697230.1:c.976C>G	ENSP00000513197.1:p.Leu326Val
ENST00000697231.1:c.971C>G	ENSP00000513198.1:n.971C>G
ENST00000697232.1:c.995C>G	ENSP00000513199.1:n.995C>G
ENST00000347310.10:c.1066C>G MANE Select	ENSP00000321345.5:p.Leu356Val
ENST00000637002.1:c.457C>G	ENSP00000490340.1:p.Leu153Val
ENST00000347310.9:c.1066C>G	ENSP00000321345.5:p.Leu356Val
ENST00000395227.2:c.-58-15638C>G	ENSP00000378652.2:n.-58-15638C>G
ENST00000425614.3:c.301C>G	ENSP00000387640.2:p.Leu101Val
ENST00000473881.2:c.191-15638C>G	ENSP00000486667.1:n.191-15638C>G
NM_144701.2:c.1066C>G	NP_653302.2:p.Leu356Val
XM_005270516.2:c.304C>G	XP_005270573.1:p.Leu102Val
XM_011540789.1:c.1156C>G	XP_011539091.1:p.Leu386Val
XM_011540790.1:c.1066C>G	XP_011539092.1:p.Leu356Val
XM_011540791.1:c.1066C>G	XP_011539093.1:p.Leu356Val
XM_011540790.3:c.1066C>G	XP_011539092.1:p.Leu356Val
XM_011540791.3:c.1066C>G	XP_011539093.1:p.Leu356Val
XR_001736993.1:n.1228+3397C>G
NM_144701.3:c.1066C>G MANE Select	NP_653302.2:p.Leu356Val