Canonical Allele Identifier: CA1002741702
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646865728
gnomAD v3: 1-67165603-T-A
gnomAD v4: 1-67165603-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67165603T>A , CM000663.2:g.67165603T>A GRCh38
NC_000001.10:g.67631286T>A , CM000663.1:g.67631286T>A GRCh37
NC_000001.9:g.67403874T>A NCBI36
NG_011498.1:g.4118T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-29-2489T>A (IL23R) ENSP00000513189.1:n.-29-2489T>A
ENST00000637002.1:c.-633-2489T>A (IL23R) ENSP00000490340.1:n.-633-2489T>A
ENST00000371007.6:c.-103-34376A>T (C1orf141) ENSP00000360046.1:n.-103-34376A>T
ENST00000448166.6:c.-103-34376A>T (C1orf141) ENSP00000415519.2:n.-103-34376A>T
XM_011540789.1:c.62-2489T>A (IL23R) XP_011539091.1:n.62-2489T>A
XM_011540790.1:c.-29-2489T>A (IL23R) XP_011539092.1:n.-29-2489T>A
XM_011540791.1:c.-29-2489T>A (IL23R) XP_011539093.1:n.-29-2489T>A
XM_011540790.3:c.-29-2489T>A (IL23R) XP_011539092.1:n.-29-2489T>A
XM_011540791.3:c.-29-2489T>A (IL23R) XP_011539093.1:n.-29-2489T>A