Canonical Allele Identifier: CA418438641
Gene: IL23R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67724430A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258747A>G , CM000663.2:g.67258747A>G GRCh38
NC_000001.10:g.67724430A>G , CM000663.1:g.67724430A>G GRCh37
NC_000001.9:g.67497018A>G NCBI36
NG_011498.1:g.97262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1348A>G ENSP00000513138.1:n.1348A>G
ENST00000697150.1:c.1406A>G ENSP00000513139.1:n.1406A>G
ENST00000697151.1:c.1339A>G ENSP00000513140.1:n.1339A>G
ENST00000697164.1:c.1419A>G ENSP00000513153.1:p.Glu473=
ENST00000697165.1:c.1206A>G ENSP00000513154.1:p.Glu402=
ENST00000347310.10:c.1509A>G MANE Select ENSP00000321345.5:p.Glu503=
ENST00000637002.1:c.900A>G ENSP00000490340.1:p.Glu300=
ENST00000347310.9:c.1509A>G ENSP00000321345.5:p.Glu503=
ENST00000395227.2:c.303A>G ENSP00000378652.2:p.Glu101=
ENST00000425614.3:c.744A>G ENSP00000387640.2:p.Glu248=
ENST00000473881.2:c.*335A>G ENSP00000486667.1:n.*335A>G
NM_144701.2:c.1509A>G NP_653302.2:p.Glu503=
XM_005270516.2:c.747A>G XP_005270573.1:p.Glu249=
XM_011540789.1:c.1599A>G XP_011539091.1:p.Glu533=
XM_011540790.1:c.1509A>G XP_011539092.1:p.Glu503=
XM_011540791.1:c.1509A>G XP_011539093.1:p.Glu503=
XM_011540790.3:c.1509A>G XP_011539092.1:p.Glu503=
XM_011540791.3:c.1509A>G XP_011539093.1:p.Glu503=
XR_001736993.1:n.1589A>G
NM_144701.3:c.1509A>G MANE Select NP_653302.2:p.Glu503=