Canonical Allele Identifier: CA899606
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs752668412
gnomAD v2: 1-67633775-A-G
gnomAD v4: 1-67168092-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67168092A>G , CM000663.2:g.67168092A>G GRCh38
NC_000001.10:g.67633775A>G , CM000663.1:g.67633775A>G GRCh37
NC_000001.9:g.67406363A>G NCBI36
NG_011498.1:g.6607A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-29A>G (IL23R) ENSP00000513189.1:n.-29A>G
ENST00000347310.10:c.-29A>G (IL23R) MANE Select ENSP00000321345.5:n.-29A>G
ENST00000637002.1:c.-633A>G (IL23R) ENSP00000490340.1:n.-633A>G
ENST00000347310.9:c.-29A>G (IL23R) ENSP00000321345.5:n.-29A>G
ENST00000371007.6:c.-103-36865T>C (C1orf141) ENSP00000360046.1:n.-103-36865T>C
ENST00000448166.6:c.-103-36865T>C (C1orf141) ENSP00000415519.2:n.-103-36865T>C
NM_144701.2:c.-29A>G (IL23R) NP_653302.2:n.-29A>G
XM_011540789.1:c.62A>G (IL23R) XP_011539091.1:p.Glu21Gly
XM_011540790.1:c.-29A>G (IL23R) XP_011539092.1:n.-29A>G
XM_011540791.1:c.-29A>G (IL23R) XP_011539093.1:n.-29A>G
XM_011540790.3:c.-29A>G (IL23R) XP_011539092.1:n.-29A>G
XM_011540791.3:c.-29A>G (IL23R) XP_011539093.1:n.-29A>G
XR_001736993.1:n.155A>G (IL23R)
NM_144701.3:c.-29A>G (IL23R) MANE Select NP_653302.2:n.-29A>G