Canonical Allele Identifier: CA340725895

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705939A>G (hg19) ; chr1:g.67240256A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240256A>G , CM000663.2:g.67240256A>G	GRCh38
NC_000001.10:g.67705939A>G , CM000663.1:g.67705939A>G	GRCh37
NC_000001.9:g.67478527A>G	NCBI36
NG_011498.1:g.78771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.999A>G	ENSP00000513137.1:n.999A>G
ENST00000697149.1:c.962A>G	ENSP00000513138.1:n.962A>G
ENST00000697150.1:c.1045+3454A>G	ENSP00000513139.1:n.1045+3454A>G
ENST00000697151.1:c.1045+3454A>G	ENSP00000513140.1:n.1045+3454A>G
ENST00000697152.1:c.799-15581A>G	ENSP00000513141.1:n.799-15581A>G
ENST00000697153.1:c.795-15581A>G	ENSP00000513142.1:n.795-15581A>G
ENST00000697154.1:c.956-18222A>G	ENSP00000513143.1:n.956-18222A>G
ENST00000697155.1:c.649-18222A>G	ENSP00000513144.1:n.649-18222A>G
ENST00000697156.1:c.1123A>G	ENSP00000513145.1:p.Ile375Val
ENST00000697157.1:c.977A>G	ENSP00000513146.1:n.977A>G
ENST00000697158.1:c.966A>G	ENSP00000513147.1:n.966A>G
ENST00000697159.1:c.816A>G	ENSP00000513148.1:n.816A>G
ENST00000697160.1:c.956-15581A>G	ENSP00000513149.1:n.956-15581A>G
ENST00000697161.1:c.659A>G	ENSP00000513150.1:n.659A>G
ENST00000697162.1:c.1052A>G	ENSP00000513151.1:n.1052A>G
ENST00000697163.1:c.1123A>G	ENSP00000513152.1:p.Ile375Val
ENST00000697164.1:c.1033A>G	ENSP00000513153.1:p.Ile345Val
ENST00000697165.1:c.820A>G	ENSP00000513154.1:p.Ile274Val
ENST00000697223.1:c.872A>G	ENSP00000513190.1:n.872A>G
ENST00000697224.1:c.884+3454A>G	ENSP00000513191.1:n.884+3454A>G
ENST00000697225.1:c.726A>G	ENSP00000513192.1:n.726A>G
ENST00000697226.1:c.738+3454A>G	ENSP00000513193.1:n.738+3454A>G
ENST00000697227.1:c.959A>G	ENSP00000513194.1:n.959A>G
ENST00000697228.1:c.815A>G	ENSP00000513195.1:n.815A>G
ENST00000697229.1:c.885-15581A>G	ENSP00000513196.1:n.885-15581A>G
ENST00000697230.1:c.1033A>G	ENSP00000513197.1:p.Ile345Val
ENST00000697231.1:c.1028A>G	ENSP00000513198.1:n.1028A>G
ENST00000697232.1:c.1052A>G	ENSP00000513199.1:n.1052A>G
ENST00000347310.10:c.1123A>G MANE Select	ENSP00000321345.5:p.Ile375Val
ENST00000637002.1:c.514A>G	ENSP00000490340.1:p.Ile172Val
ENST00000347310.9:c.1123A>G	ENSP00000321345.5:p.Ile375Val
ENST00000395227.2:c.-58-15581A>G	ENSP00000378652.2:n.-58-15581A>G
ENST00000425614.3:c.358A>G	ENSP00000387640.2:p.Ile120Val
ENST00000473881.2:c.191-15581A>G	ENSP00000486667.1:n.191-15581A>G
NM_144701.2:c.1123A>G	NP_653302.2:p.Ile375Val
XM_005270516.2:c.361A>G	XP_005270573.1:p.Ile121Val
XM_011540789.1:c.1213A>G	XP_011539091.1:p.Ile405Val
XM_011540790.1:c.1123A>G	XP_011539092.1:p.Ile375Val
XM_011540791.1:c.1123A>G	XP_011539093.1:p.Ile375Val
XM_011540790.3:c.1123A>G	XP_011539092.1:p.Ile375Val
XM_011540791.3:c.1123A>G	XP_011539093.1:p.Ile375Val
XR_001736993.1:n.1228+3454A>G
NM_144701.3:c.1123A>G MANE Select	NP_653302.2:p.Ile375Val