Canonical Allele Identifier: CA418438822
Gene: IL23R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67724775A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259092A>G , CM000663.2:g.67259092A>G GRCh38
NC_000001.10:g.67724775A>G , CM000663.1:g.67724775A>G GRCh37
NC_000001.9:g.67497363A>G NCBI36
NG_011498.1:g.97607A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1693A>G ENSP00000513138.1:n.1693A>G
ENST00000697150.1:c.1751A>G ENSP00000513139.1:n.1751A>G
ENST00000697151.1:c.1684A>G ENSP00000513140.1:n.1684A>G
ENST00000697164.1:c.1764A>G ENSP00000513153.1:p.Glu588=
ENST00000697165.1:c.1551A>G ENSP00000513154.1:p.Glu517=
ENST00000347310.10:c.1854A>G MANE Select ENSP00000321345.5:p.Glu618=
ENST00000637002.1:c.1245A>G ENSP00000490340.1:p.Glu415=
ENST00000347310.9:c.1854A>G ENSP00000321345.5:p.Glu618=
ENST00000395227.2:c.648A>G ENSP00000378652.2:p.Glu216=
ENST00000425614.3:c.1089A>G ENSP00000387640.2:p.Glu363=
ENST00000473881.2:c.*680A>G ENSP00000486667.1:n.*680A>G
NM_144701.2:c.1854A>G NP_653302.2:p.Glu618=
XM_005270516.2:c.1092A>G XP_005270573.1:p.Glu364=
XM_011540789.1:c.1944A>G XP_011539091.1:p.Glu648=
XM_011540790.1:c.1854A>G XP_011539092.1:p.Glu618=
XM_011540791.1:c.1854A>G XP_011539093.1:p.Glu618=
XM_011540790.3:c.1854A>G XP_011539092.1:p.Glu618=
XM_011540791.3:c.1854A>G XP_011539093.1:p.Glu618=
XR_001736993.1:n.1934A>G
NM_144701.3:c.1854A>G MANE Select NP_653302.2:p.Glu618=