Canonical Allele Identifier: CA23537422
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs117633859
gnomAD v2: 1-67627828-A-G
gnomAD v3: 1-67162145-A-G
gnomAD v4: 1-67162145-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67162145A>G , CM000663.2:g.67162145A>G GRCh38
NC_000001.10:g.67627828A>G , CM000663.1:g.67627828A>G GRCh37
NC_000001.9:g.67400416A>G NCBI36
NG_011498.1:g.660A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697222.1:c.-29-5947A>G (IL23R) ENSP00000513189.1:n.-29-5947A>G
ENST00000637002.1:c.-633-5947A>G (IL23R) ENSP00000490340.1:n.-633-5947A>G
ENST00000371007.6:c.-103-30918T>C (C1orf141) ENSP00000360046.1:n.-103-30918T>C
ENST00000448166.6:c.-103-30918T>C (C1orf141) ENSP00000415519.2:n.-103-30918T>C
XM_011540789.1:c.62-5947A>G (IL23R) XP_011539091.1:n.62-5947A>G
XM_011540790.1:c.-29-5947A>G (IL23R) XP_011539092.1:n.-29-5947A>G
XM_011540791.1:c.-30+1318A>G (IL23R) XP_011539093.1:n.-30+1318A>G
XM_011540790.3:c.-29-5947A>G (IL23R) XP_011539092.1:n.-29-5947A>G
XM_011540791.3:c.-30+1318A>G (IL23R) XP_011539093.1:n.-30+1318A>G