Canonical Allele Identifier: CA418269039

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705962T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240279T>G , CM000663.2:g.67240279T>G	GRCh38
NC_000001.10:g.67705962T>G , CM000663.1:g.67705962T>G	GRCh37
NC_000001.9:g.67478550T>G	NCBI36
NG_011498.1:g.78794T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.1022T>G	ENSP00000513137.1:n.1022T>G
ENST00000697149.1:c.985T>G	ENSP00000513138.1:n.985T>G
ENST00000697150.1:c.1045+3477T>G	ENSP00000513139.1:n.1045+3477T>G
ENST00000697151.1:c.1045+3477T>G	ENSP00000513140.1:n.1045+3477T>G
ENST00000697152.1:c.799-15558T>G	ENSP00000513141.1:n.799-15558T>G
ENST00000697153.1:c.795-15558T>G	ENSP00000513142.1:n.795-15558T>G
ENST00000697154.1:c.956-18199T>G	ENSP00000513143.1:n.956-18199T>G
ENST00000697155.1:c.649-18199T>G	ENSP00000513144.1:n.649-18199T>G
ENST00000697156.1:c.1146T>G	ENSP00000513145.1:p.Thr382=
ENST00000697157.1:c.1000T>G	ENSP00000513146.1:n.1000T>G
ENST00000697158.1:c.989T>G	ENSP00000513147.1:n.989T>G
ENST00000697159.1:c.839T>G	ENSP00000513148.1:n.839T>G
ENST00000697160.1:c.956-15558T>G	ENSP00000513149.1:n.956-15558T>G
ENST00000697161.1:c.682T>G	ENSP00000513150.1:n.682T>G
ENST00000697162.1:c.1075T>G	ENSP00000513151.1:n.1075T>G
ENST00000697163.1:c.1146T>G	ENSP00000513152.1:p.Thr382=
ENST00000697164.1:c.1056T>G	ENSP00000513153.1:p.Thr352=
ENST00000697165.1:c.843T>G	ENSP00000513154.1:p.Thr281=
ENST00000697223.1:c.895T>G	ENSP00000513190.1:n.895T>G
ENST00000697224.1:c.884+3477T>G	ENSP00000513191.1:n.884+3477T>G
ENST00000697225.1:c.749T>G	ENSP00000513192.1:n.749T>G
ENST00000697226.1:c.738+3477T>G	ENSP00000513193.1:n.738+3477T>G
ENST00000697227.1:c.982T>G	ENSP00000513194.1:n.982T>G
ENST00000697228.1:c.838T>G	ENSP00000513195.1:n.838T>G
ENST00000697229.1:c.885-15558T>G	ENSP00000513196.1:n.885-15558T>G
ENST00000697230.1:c.1056T>G	ENSP00000513197.1:p.Thr352=
ENST00000697231.1:c.1051T>G	ENSP00000513198.1:n.1051T>G
ENST00000697232.1:c.1075T>G	ENSP00000513199.1:n.1075T>G
ENST00000347310.10:c.1146T>G MANE Select	ENSP00000321345.5:p.Thr382=
ENST00000637002.1:c.537T>G	ENSP00000490340.1:p.Thr179=
ENST00000347310.9:c.1146T>G	ENSP00000321345.5:p.Thr382=
ENST00000395227.2:c.-58-15558T>G	ENSP00000378652.2:n.-58-15558T>G
ENST00000425614.3:c.381T>G	ENSP00000387640.2:p.Thr127=
ENST00000473881.2:c.191-15558T>G	ENSP00000486667.1:n.191-15558T>G
NM_144701.2:c.1146T>G	NP_653302.2:p.Thr382=
XM_005270516.2:c.384T>G	XP_005270573.1:p.Thr128=
XM_011540789.1:c.1236T>G	XP_011539091.1:p.Thr412=
XM_011540790.1:c.1146T>G	XP_011539092.1:p.Thr382=
XM_011540791.1:c.1146T>G	XP_011539093.1:p.Thr382=
XM_011540790.3:c.1146T>G	XP_011539092.1:p.Thr382=
XM_011540791.3:c.1146T>G	XP_011539093.1:p.Thr382=
XR_001736993.1:n.1228+3477T>G
NM_144701.3:c.1146T>G MANE Select	NP_653302.2:p.Thr382=