Canonical Allele Identifier: CA1002754251
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs1653109697
gnomAD v3: 1-67259151-T-C
gnomAD v4: 1-67259151-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259151T>C , CM000663.2:g.67259151T>C GRCh38
NC_000001.10:g.67724834T>C , CM000663.1:g.67724834T>C GRCh37
NC_000001.9:g.67497422T>C NCBI36
NG_011498.1:g.97666T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*23T>C MANE Select ENSP00000321345.5:n.*23T>C
ENST00000637002.1:c.*23T>C ENSP00000490340.1:n.*23T>C
ENST00000347310.9:c.*23T>C ENSP00000321345.5:n.*23T>C
ENST00000395227.2:c.*23T>C ENSP00000378652.2:n.*23T>C
ENST00000425614.3:c.*23T>C ENSP00000387640.2:n.*23T>C
ENST00000473881.2:c.*739T>C ENSP00000486667.1:n.*739T>C
NM_144701.2:c.*23T>C NP_653302.2:n.*23T>C
XM_005270516.2:c.*23T>C XP_005270573.1:n.*23T>C
XM_011540789.1:c.*23T>C XP_011539091.1:n.*23T>C
XM_011540790.1:c.*23T>C XP_011539092.1:n.*23T>C
XM_011540791.1:c.*23T>C XP_011539093.1:n.*23T>C
XM_011540790.3:c.*23T>C XP_011539092.1:n.*23T>C
XM_011540791.3:c.*23T>C XP_011539093.1:n.*23T>C
NM_144701.3:c.*23T>C MANE Select NP_653302.2:n.*23T>C
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