Canonical Allele Identifier: CA1173064354
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259117T= , CM000663.2:g.67259117T= GRCh38
NC_000001.10:g.67724800T= , CM000663.1:g.67724800T= GRCh37
NC_000001.9:g.67497388T= NCBI36
NG_011498.1:g.97632T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697149.1:c.1718T= ENSP00000513138.1:n.1718T=
ENST00000697150.1:c.1776T= ENSP00000513139.1:n.1776T=
ENST00000697151.1:c.1709T= ENSP00000513140.1:n.1709T=
ENST00000697164.1:c.1789T= ENSP00000513153.1:p.Leu597=
ENST00000697165.1:c.1576T= ENSP00000513154.1:p.Leu526=
ENST00000347310.10:c.1879T= MANE Select ENSP00000321345.5:p.Leu627=
ENST00000637002.1:c.1270T= ENSP00000490340.1:p.Leu424=
ENST00000347310.9:c.1879T= ENSP00000321345.5:p.Leu627=
ENST00000395227.2:c.673T= ENSP00000378652.2:p.Leu225=
ENST00000425614.3:c.1114T= ENSP00000387640.2:p.Leu372=
ENST00000473881.2:c.*705T= ENSP00000486667.1:n.*705T=
NM_144701.2:c.1879T= NP_653302.2:p.Leu627=
XM_005270516.2:c.1117T= XP_005270573.1:p.Leu373=
XM_011540789.1:c.1969T= XP_011539091.1:p.Leu657=
XM_011540790.1:c.1879T= XP_011539092.1:p.Leu627=
XM_011540791.1:c.1879T= XP_011539093.1:p.Leu627=
XM_011540790.3:c.1879T= XP_011539092.1:p.Leu627=
XM_011540791.3:c.1879T= XP_011539093.1:p.Leu627=
XR_001736993.1:n.1959T=
NM_144701.3:c.1879T= MANE Select NP_653302.2:p.Leu627=