Canonical Allele Identifier: CA2841561806
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67228406C>T , CM000663.2:g.67228406C>T GRCh38
NC_000001.10:g.67694089C>T , CM000663.1:g.67694089C>T GRCh37
NC_000001.9:g.67466677C>T NCBI36
NG_011498.1:g.66921C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.832-8307C>T (IL23R) ENSP00000513137.1:n.832-8307C>T
ENST00000697149.1:c.795-8307C>T (IL23R) ENSP00000513138.1:n.795-8307C>T
ENST00000697150.1:c.956-8307C>T (IL23R) ENSP00000513139.1:n.956-8307C>T
ENST00000697151.1:c.956-8307C>T (IL23R) ENSP00000513140.1:n.956-8307C>T
ENST00000697152.1:c.798+21351C>T (IL23R) ENSP00000513141.1:n.798+21351C>T
ENST00000697153.1:c.794+8676C>T (IL23R) ENSP00000513142.1:n.794+8676C>T
ENST00000697154.1:c.955+8676C>T (IL23R) ENSP00000513143.1:n.955+8676C>T
ENST00000697155.1:c.648+8676C>T (IL23R) ENSP00000513144.1:n.648+8676C>T
ENST00000697156.1:c.956-8307C>T (IL23R) ENSP00000513145.1:n.956-8307C>T
ENST00000697157.1:c.810-8307C>T (IL23R) ENSP00000513146.1:n.810-8307C>T
ENST00000697158.1:c.799-8307C>T (IL23R) ENSP00000513147.1:n.799-8307C>T
ENST00000697159.1:c.649-8307C>T (IL23R) ENSP00000513148.1:n.649-8307C>T
ENST00000697160.1:c.955+8676C>T (IL23R) ENSP00000513149.1:n.955+8676C>T
ENST00000697161.1:c.492-8307C>T (IL23R) ENSP00000513150.1:n.492-8307C>T
ENST00000697162.1:c.885-8307C>T (IL23R) ENSP00000513151.1:n.885-8307C>T
ENST00000697163.1:c.956-8307C>T (IL23R) ENSP00000513152.1:n.956-8307C>T
ENST00000697164.1:c.955+8676C>T (IL23R) ENSP00000513153.1:n.955+8676C>T
ENST00000697165.1:c.653-8307C>T (IL23R) ENSP00000513154.1:n.653-8307C>T
ENST00000697223.1:c.794+8676C>T (IL23R) ENSP00000513190.1:n.794+8676C>T
ENST00000697224.1:c.795-8307C>T (IL23R) ENSP00000513191.1:n.795-8307C>T
ENST00000697225.1:c.648+8676C>T (IL23R) ENSP00000513192.1:n.648+8676C>T
ENST00000697226.1:c.649-8307C>T (IL23R) ENSP00000513193.1:n.649-8307C>T
ENST00000697227.1:c.867-8382C>T (IL23R) ENSP00000513194.1:n.867-8382C>T
ENST00000697228.1:c.648-8307C>T (IL23R) ENSP00000513195.1:n.648-8307C>T
ENST00000697229.1:c.884+8676C>T (IL23R) ENSP00000513196.1:n.884+8676C>T
ENST00000697230.1:c.955+8676C>T (IL23R) ENSP00000513197.1:n.955+8676C>T
ENST00000697231.1:c.950+8676C>T (IL23R) ENSP00000513198.1:n.950+8676C>T
ENST00000697232.1:c.885-8307C>T (IL23R) ENSP00000513199.1:n.885-8307C>T
ENST00000347310.10:c.956-8307C>T (IL23R) MANE Select ENSP00000321345.5:n.956-8307C>T
ENST00000637002.1:c.347-8307C>T (IL23R) ENSP00000490340.1:n.347-8307C>T
ENST00000347310.9:c.956-8307C>T (IL23R) ENSP00000321345.5:n.956-8307C>T
ENST00000371007.6:c.-104+3440G>A (C1orf141) ENSP00000360046.1:n.-104+3440G>A
ENST00000395227.2:c.-59+8676C>T (IL23R) ENSP00000378652.2:n.-59+8676C>T
ENST00000425614.3:c.191-8307C>T (IL23R) ENSP00000387640.2:n.191-8307C>T
ENST00000448166.6:c.-104+3440G>A (C1orf141) ENSP00000415519.2:n.-104+3440G>A
ENST00000473881.2:c.190+8676C>T (IL23R) ENSP00000486667.1:n.190+8676C>T
NM_144701.2:c.956-8307C>T (IL23R) NP_653302.2:n.956-8307C>T
XM_005270516.2:c.194-8307C>T (IL23R) XP_005270573.1:n.194-8307C>T
XM_011540789.1:c.1046-8307C>T (IL23R) XP_011539091.1:n.1046-8307C>T
XM_011540790.1:c.956-8307C>T (IL23R) XP_011539092.1:n.956-8307C>T
XM_011540791.1:c.956-8307C>T (IL23R) XP_011539093.1:n.956-8307C>T
XM_011540790.3:c.956-8307C>T (IL23R) XP_011539092.1:n.956-8307C>T
XM_011540791.3:c.956-8307C>T (IL23R) XP_011539093.1:n.956-8307C>T
XR_001736993.1:n.1139-8307C>T (IL23R)
NM_144701.3:c.956-8307C>T (IL23R) MANE Select NP_653302.2:n.956-8307C>T