Canonical Allele Identifier: CA1173064498
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259466C= , CM000663.2:g.67259466C= GRCh38
NC_000001.10:g.67725149C= , CM000663.1:g.67725149C= GRCh37
NC_000001.9:g.67497737C= NCBI36
NG_011498.1:g.97981C=

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*338C= MANE Select ENSP00000321345.5:n.*338C=
ENST00000347310.9:c.*338C= ENSP00000321345.5:n.*338C=
ENST00000395227.2:c.*338C= ENSP00000378652.2:n.*338C=
ENST00000473881.2:c.*1054C= ENSP00000486667.1:n.*1054C=
NM_144701.2:c.*338C= NP_653302.2:n.*338C=
XM_005270516.2:c.*338C= XP_005270573.1:n.*338C=
XM_011540789.1:c.*338C= XP_011539091.1:n.*338C=
XM_011540790.1:c.*338C= XP_011539092.1:n.*338C=
XM_011540791.1:c.*338C= XP_011539093.1:n.*338C=
XM_011540790.3:c.*338C= XP_011539092.1:n.*338C=
XM_011540791.3:c.*338C= XP_011539093.1:n.*338C=
NM_144701.3:c.*338C= MANE Select NP_653302.2:n.*338C=