Canonical Allele Identifier: CA1173064381
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259194T= , CM000663.2:g.67259194T= GRCh38
NC_000001.10:g.67724877T= , CM000663.1:g.67724877T= GRCh37
NC_000001.9:g.67497465T= NCBI36
NG_011498.1:g.97709T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*66T= MANE Select ENSP00000321345.5:n.*66T=
ENST00000347310.9:c.*66T= ENSP00000321345.5:n.*66T=
ENST00000395227.2:c.*66T= ENSP00000378652.2:n.*66T=
ENST00000425614.3:c.*66T= ENSP00000387640.2:n.*66T=
ENST00000473881.2:c.*782T= ENSP00000486667.1:n.*782T=
NM_144701.2:c.*66T= NP_653302.2:n.*66T=
XM_005270516.2:c.*66T= XP_005270573.1:n.*66T=
XM_011540789.1:c.*66T= XP_011539091.1:n.*66T=
XM_011540790.1:c.*66T= XP_011539092.1:n.*66T=
XM_011540791.1:c.*66T= XP_011539093.1:n.*66T=
XM_011540790.3:c.*66T= XP_011539092.1:n.*66T=
XM_011540791.3:c.*66T= XP_011539093.1:n.*66T=
NM_144701.3:c.*66T= MANE Select NP_653302.2:n.*66T=