Canonical Allele Identifier: CA913266393
Gene: IL23R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259228G>A , CM000663.2:g.67259228G>A GRCh38
NC_000001.10:g.67724911G>A , CM000663.1:g.67724911G>A GRCh37
NC_000001.9:g.67497499G>A NCBI36
NG_011498.1:g.97743G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*100G>A MANE Select ENSP00000321345.5:n.*100G>A
ENST00000347310.9:c.*100G>A ENSP00000321345.5:n.*100G>A
ENST00000395227.2:c.*100G>A ENSP00000378652.2:n.*100G>A
ENST00000425614.3:c.*100G>A ENSP00000387640.2:n.*100G>A
ENST00000473881.2:c.*816G>A ENSP00000486667.1:n.*816G>A
NM_144701.2:c.*100G>A NP_653302.2:n.*100G>A
XM_005270516.2:c.*100G>A XP_005270573.1:n.*100G>A
XM_011540789.1:c.*100G>A XP_011539091.1:n.*100G>A
XM_011540790.1:c.*100G>A XP_011539092.1:n.*100G>A
XM_011540791.1:c.*100G>A XP_011539093.1:n.*100G>A
XM_011540790.3:c.*100G>A XP_011539092.1:n.*100G>A
XM_011540791.3:c.*100G>A XP_011539093.1:n.*100G>A
NM_144701.3:c.*100G>A MANE Select NP_653302.2:n.*100G>A
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