Canonical Allele Identifier: CA23535454
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs529831663

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67209768C>T , CM000663.2:g.67209768C>T GRCh38
NC_000001.10:g.67675451C>T , CM000663.1:g.67675451C>T GRCh37
NC_000001.9:g.67448039C>T NCBI36
NG_011498.1:g.48283C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.674+2713C>T (IL23R) ENSP00000513137.1:n.674+2713C>T
ENST00000697149.1:c.637+2713C>T (IL23R) ENSP00000513138.1:n.637+2713C>T
ENST00000697150.1:c.798+2713C>T (IL23R) ENSP00000513139.1:n.798+2713C>T
ENST00000697151.1:c.798+2713C>T (IL23R) ENSP00000513140.1:n.798+2713C>T
ENST00000697152.1:c.798+2713C>T (IL23R) ENSP00000513141.1:n.798+2713C>T
ENST00000697153.1:c.637+2713C>T (IL23R) ENSP00000513142.1:n.637+2713C>T
ENST00000697154.1:c.798+2713C>T (IL23R) ENSP00000513143.1:n.798+2713C>T
ENST00000697155.1:c.492-9806C>T (IL23R) ENSP00000513144.1:n.492-9806C>T
ENST00000697156.1:c.798+2713C>T (IL23R) ENSP00000513145.1:n.798+2713C>T
ENST00000697157.1:c.652+8871C>T (IL23R) ENSP00000513146.1:n.652+8871C>T
ENST00000697158.1:c.798+2713C>T (IL23R) ENSP00000513147.1:n.798+2713C>T
ENST00000697159.1:c.492-9806C>T (IL23R) ENSP00000513148.1:n.492-9806C>T
ENST00000697160.1:c.798+2713C>T (IL23R) ENSP00000513149.1:n.798+2713C>T
ENST00000697161.1:c.491+26809C>T (IL23R) ENSP00000513150.1:n.491+26809C>T
ENST00000697162.1:c.727+2713C>T (IL23R) ENSP00000513151.1:n.727+2713C>T
ENST00000697163.1:c.798+2713C>T (IL23R) ENSP00000513152.1:n.798+2713C>T
ENST00000697164.1:c.798+2713C>T (IL23R) ENSP00000513153.1:n.798+2713C>T
ENST00000697165.1:c.652+8871C>T (IL23R) ENSP00000513154.1:n.652+8871C>T
ENST00000697223.1:c.637+2713C>T (IL23R) ENSP00000513190.1:n.637+2713C>T
ENST00000697224.1:c.637+2713C>T (IL23R) ENSP00000513191.1:n.637+2713C>T
ENST00000697225.1:c.492-9806C>T (IL23R) ENSP00000513192.1:n.492-9806C>T
ENST00000697226.1:c.492-9806C>T (IL23R) ENSP00000513193.1:n.492-9806C>T
ENST00000697227.1:c.798+2713C>T (IL23R) ENSP00000513194.1:n.798+2713C>T
ENST00000697228.1:c.647+8871C>T (IL23R) ENSP00000513195.1:n.647+8871C>T
ENST00000697229.1:c.727+2713C>T (IL23R) ENSP00000513196.1:n.727+2713C>T
ENST00000697230.1:c.798+2713C>T (IL23R) ENSP00000513197.1:n.798+2713C>T
ENST00000697231.1:c.793+2713C>T (IL23R) ENSP00000513198.1:n.793+2713C>T
ENST00000697232.1:c.727+2713C>T (IL23R) ENSP00000513199.1:n.727+2713C>T
ENST00000347310.10:c.798+2713C>T (IL23R) MANE Select ENSP00000321345.5:n.798+2713C>T
ENST00000637002.1:c.189+2713C>T (IL23R) ENSP00000490340.1:n.189+2713C>T
ENST00000347310.9:c.798+2713C>T (IL23R) ENSP00000321345.5:n.798+2713C>T
ENST00000371007.6:c.-104+22078G>A (C1orf141) ENSP00000360046.1:n.-104+22078G>A
ENST00000425614.3:c.33+2070C>T (IL23R) ENSP00000387640.2:n.33+2070C>T
ENST00000448166.6:c.-104+22078G>A (C1orf141) ENSP00000415519.2:n.-104+22078G>A
ENST00000473881.2:c.33+2070C>T (IL23R) ENSP00000486667.1:n.33+2070C>T
NM_144701.2:c.798+2713C>T (IL23R) NP_653302.2:n.798+2713C>T
XM_005270516.2:c.36+2713C>T (IL23R) XP_005270573.1:n.36+2713C>T
XM_011540789.1:c.888+2713C>T (IL23R) XP_011539091.1:n.888+2713C>T
XM_011540790.1:c.798+2713C>T (IL23R) XP_011539092.1:n.798+2713C>T
XM_011540791.1:c.798+2713C>T (IL23R) XP_011539093.1:n.798+2713C>T
XM_011540790.3:c.798+2713C>T (IL23R) XP_011539092.1:n.798+2713C>T
XM_011540791.3:c.798+2713C>T (IL23R) XP_011539093.1:n.798+2713C>T
XR_001736993.1:n.981+2713C>T (IL23R)
NM_144701.3:c.798+2713C>T (IL23R) MANE Select NP_653302.2:n.798+2713C>T