Canonical Allele Identifier: CA418269002

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705911T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240228T>A , CM000663.2:g.67240228T>A	GRCh38
NC_000001.10:g.67705911T>A , CM000663.1:g.67705911T>A	GRCh37
NC_000001.9:g.67478499T>A	NCBI36
NG_011498.1:g.78743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.971T>A	ENSP00000513137.1:n.971T>A
ENST00000697149.1:c.934T>A	ENSP00000513138.1:n.934T>A
ENST00000697150.1:c.1045+3426T>A	ENSP00000513139.1:n.1045+3426T>A
ENST00000697151.1:c.1045+3426T>A	ENSP00000513140.1:n.1045+3426T>A
ENST00000697152.1:c.799-15609T>A	ENSP00000513141.1:n.799-15609T>A
ENST00000697153.1:c.795-15609T>A	ENSP00000513142.1:n.795-15609T>A
ENST00000697154.1:c.956-18250T>A	ENSP00000513143.1:n.956-18250T>A
ENST00000697155.1:c.649-18250T>A	ENSP00000513144.1:n.649-18250T>A
ENST00000697156.1:c.1095T>A	ENSP00000513145.1:p.Val365=
ENST00000697157.1:c.949T>A	ENSP00000513146.1:n.949T>A
ENST00000697158.1:c.938T>A	ENSP00000513147.1:n.938T>A
ENST00000697159.1:c.788T>A	ENSP00000513148.1:n.788T>A
ENST00000697160.1:c.956-15609T>A	ENSP00000513149.1:n.956-15609T>A
ENST00000697161.1:c.631T>A	ENSP00000513150.1:n.631T>A
ENST00000697162.1:c.1024T>A	ENSP00000513151.1:n.1024T>A
ENST00000697163.1:c.1095T>A	ENSP00000513152.1:p.Val365=
ENST00000697164.1:c.1005T>A	ENSP00000513153.1:p.Val335=
ENST00000697165.1:c.792T>A	ENSP00000513154.1:p.Val264=
ENST00000697223.1:c.844T>A	ENSP00000513190.1:n.844T>A
ENST00000697224.1:c.884+3426T>A	ENSP00000513191.1:n.884+3426T>A
ENST00000697225.1:c.698T>A	ENSP00000513192.1:n.698T>A
ENST00000697226.1:c.738+3426T>A	ENSP00000513193.1:n.738+3426T>A
ENST00000697227.1:c.931T>A	ENSP00000513194.1:n.931T>A
ENST00000697228.1:c.787T>A	ENSP00000513195.1:n.787T>A
ENST00000697229.1:c.885-15609T>A	ENSP00000513196.1:n.885-15609T>A
ENST00000697230.1:c.1005T>A	ENSP00000513197.1:p.Val335=
ENST00000697231.1:c.1000T>A	ENSP00000513198.1:n.1000T>A
ENST00000697232.1:c.1024T>A	ENSP00000513199.1:n.1024T>A
ENST00000347310.10:c.1095T>A MANE Select	ENSP00000321345.5:p.Val365=
ENST00000637002.1:c.486T>A	ENSP00000490340.1:p.Val162=
ENST00000347310.9:c.1095T>A	ENSP00000321345.5:p.Val365=
ENST00000395227.2:c.-58-15609T>A	ENSP00000378652.2:n.-58-15609T>A
ENST00000425614.3:c.330T>A	ENSP00000387640.2:p.Val110=
ENST00000473881.2:c.191-15609T>A	ENSP00000486667.1:n.191-15609T>A
NM_144701.2:c.1095T>A	NP_653302.2:p.Val365=
XM_005270516.2:c.333T>A	XP_005270573.1:p.Val111=
XM_011540789.1:c.1185T>A	XP_011539091.1:p.Val395=
XM_011540790.1:c.1095T>A	XP_011539092.1:p.Val365=
XM_011540791.1:c.1095T>A	XP_011539093.1:p.Val365=
XM_011540790.3:c.1095T>A	XP_011539092.1:p.Val365=
XM_011540791.3:c.1095T>A	XP_011539093.1:p.Val365=
XR_001736993.1:n.1228+3426T>A
NM_144701.3:c.1095T>A MANE Select	NP_653302.2:p.Val365=