Canonical Allele Identifier: CA418438840
Gene: IL23R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67724805A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259122A>G , CM000663.2:g.67259122A>G GRCh38
NC_000001.10:g.67724805A>G , CM000663.1:g.67724805A>G GRCh37
NC_000001.9:g.67497393A>G NCBI36
NG_011498.1:g.97637A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697149.1:c.1723A>G ENSP00000513138.1:n.1723A>G
ENST00000697150.1:c.1781A>G ENSP00000513139.1:n.1781A>G
ENST00000697151.1:c.1714A>G ENSP00000513140.1:n.1714A>G
ENST00000697164.1:c.1794A>G ENSP00000513153.1:p.Glu598=
ENST00000697165.1:c.1581A>G ENSP00000513154.1:p.Glu527=
ENST00000347310.10:c.1884A>G MANE Select ENSP00000321345.5:p.Glu628=
ENST00000637002.1:c.1275A>G ENSP00000490340.1:p.Glu425=
ENST00000347310.9:c.1884A>G ENSP00000321345.5:p.Glu628=
ENST00000395227.2:c.678A>G ENSP00000378652.2:p.Glu226=
ENST00000425614.3:c.1119A>G ENSP00000387640.2:p.Glu373=
ENST00000473881.2:c.*710A>G ENSP00000486667.1:n.*710A>G
NM_144701.2:c.1884A>G NP_653302.2:p.Glu628=
XM_005270516.2:c.1122A>G XP_005270573.1:p.Glu374=
XM_011540789.1:c.1974A>G XP_011539091.1:p.Glu658=
XM_011540790.1:c.1884A>G XP_011539092.1:p.Glu628=
XM_011540791.1:c.1884A>G XP_011539093.1:p.Glu628=
XM_011540790.3:c.1884A>G XP_011539092.1:p.Glu628=
XM_011540791.3:c.1884A>G XP_011539093.1:p.Glu628=
XR_001736993.1:n.1964A>G
NM_144701.3:c.1884A>G MANE Select NP_653302.2:p.Glu628=