Canonical Allele Identifier: CA1173049041
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1650377156

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67222720A>G , CM000663.2:g.67222720A>G GRCh38
NC_000001.10:g.67688403A>G , CM000663.1:g.67688403A>G GRCh37
NC_000001.9:g.67460991A>G NCBI36
NG_011498.1:g.61235A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.831+2990A>G (IL23R) ENSP00000513137.1:n.831+2990A>G
ENST00000697149.1:c.794+2990A>G (IL23R) ENSP00000513138.1:n.794+2990A>G
ENST00000697150.1:c.955+2990A>G (IL23R) ENSP00000513139.1:n.955+2990A>G
ENST00000697151.1:c.955+2990A>G (IL23R) ENSP00000513140.1:n.955+2990A>G
ENST00000697152.1:c.798+15665A>G (IL23R) ENSP00000513141.1:n.798+15665A>G
ENST00000697153.1:c.794+2990A>G (IL23R) ENSP00000513142.1:n.794+2990A>G
ENST00000697154.1:c.955+2990A>G (IL23R) ENSP00000513143.1:n.955+2990A>G
ENST00000697155.1:c.648+2990A>G (IL23R) ENSP00000513144.1:n.648+2990A>G
ENST00000697156.1:c.955+2990A>G (IL23R) ENSP00000513145.1:n.955+2990A>G
ENST00000697157.1:c.809+2990A>G (IL23R) ENSP00000513146.1:n.809+2990A>G
ENST00000697158.1:c.799-13993A>G (IL23R) ENSP00000513147.1:n.799-13993A>G
ENST00000697159.1:c.648+2990A>G (IL23R) ENSP00000513148.1:n.648+2990A>G
ENST00000697160.1:c.955+2990A>G (IL23R) ENSP00000513149.1:n.955+2990A>G
ENST00000697161.1:c.492-13993A>G (IL23R) ENSP00000513150.1:n.492-13993A>G
ENST00000697162.1:c.884+2990A>G (IL23R) ENSP00000513151.1:n.884+2990A>G
ENST00000697163.1:c.955+2990A>G (IL23R) ENSP00000513152.1:n.955+2990A>G
ENST00000697164.1:c.955+2990A>G (IL23R) ENSP00000513153.1:n.955+2990A>G
ENST00000697165.1:c.653-13993A>G (IL23R) ENSP00000513154.1:n.653-13993A>G
ENST00000697223.1:c.794+2990A>G (IL23R) ENSP00000513190.1:n.794+2990A>G
ENST00000697224.1:c.794+2990A>G (IL23R) ENSP00000513191.1:n.794+2990A>G
ENST00000697225.1:c.648+2990A>G (IL23R) ENSP00000513192.1:n.648+2990A>G
ENST00000697226.1:c.648+2990A>G (IL23R) ENSP00000513193.1:n.648+2990A>G
ENST00000697227.1:c.866+3079A>G (IL23R) ENSP00000513194.1:n.866+3079A>G
ENST00000697228.1:c.648-13993A>G (IL23R) ENSP00000513195.1:n.648-13993A>G
ENST00000697229.1:c.884+2990A>G (IL23R) ENSP00000513196.1:n.884+2990A>G
ENST00000697230.1:c.955+2990A>G (IL23R) ENSP00000513197.1:n.955+2990A>G
ENST00000697231.1:c.950+2990A>G (IL23R) ENSP00000513198.1:n.950+2990A>G
ENST00000697232.1:c.884+2990A>G (IL23R) ENSP00000513199.1:n.884+2990A>G
ENST00000347310.10:c.955+2990A>G (IL23R) MANE Select ENSP00000321345.5:n.955+2990A>G
ENST00000637002.1:c.346+2990A>G (IL23R) ENSP00000490340.1:n.346+2990A>G
ENST00000347310.9:c.955+2990A>G (IL23R) ENSP00000321345.5:n.955+2990A>G
ENST00000371007.6:c.-104+9126T>C (C1orf141) ENSP00000360046.1:n.-104+9126T>C
ENST00000395227.2:c.-59+2990A>G (IL23R) ENSP00000378652.2:n.-59+2990A>G
ENST00000425614.3:c.190+2990A>G (IL23R) ENSP00000387640.2:n.190+2990A>G
ENST00000448166.6:c.-104+9126T>C (C1orf141) ENSP00000415519.2:n.-104+9126T>C
ENST00000473881.2:c.190+2990A>G (IL23R) ENSP00000486667.1:n.190+2990A>G
NM_144701.2:c.955+2990A>G (IL23R) NP_653302.2:n.955+2990A>G
XM_005270516.2:c.193+2990A>G (IL23R) XP_005270573.1:n.193+2990A>G
XM_011540789.1:c.1045+2990A>G (IL23R) XP_011539091.1:n.1045+2990A>G
XM_011540790.1:c.955+2990A>G (IL23R) XP_011539092.1:n.955+2990A>G
XM_011540791.1:c.955+2990A>G (IL23R) XP_011539093.1:n.955+2990A>G
XM_011540790.3:c.955+2990A>G (IL23R) XP_011539092.1:n.955+2990A>G
XM_011540791.3:c.955+2990A>G (IL23R) XP_011539093.1:n.955+2990A>G
XR_001736993.1:n.1138+2990A>G (IL23R)
NM_144701.3:c.955+2990A>G (IL23R) MANE Select NP_653302.2:n.955+2990A>G