Canonical Allele Identifier: CA418438733
Gene: IL23R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67724493A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258810A>G , CM000663.2:g.67258810A>G GRCh38
NC_000001.10:g.67724493A>G , CM000663.1:g.67724493A>G GRCh37
NC_000001.9:g.67497081A>G NCBI36
NG_011498.1:g.97325A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1411A>G ENSP00000513138.1:n.1411A>G
ENST00000697150.1:c.1469A>G ENSP00000513139.1:n.1469A>G
ENST00000697151.1:c.1402A>G ENSP00000513140.1:n.1402A>G
ENST00000697164.1:c.1482A>G ENSP00000513153.1:p.Leu494=
ENST00000697165.1:c.1269A>G ENSP00000513154.1:p.Leu423=
ENST00000347310.10:c.1572A>G MANE Select ENSP00000321345.5:p.Leu524=
ENST00000637002.1:c.963A>G ENSP00000490340.1:p.Leu321=
ENST00000347310.9:c.1572A>G ENSP00000321345.5:p.Leu524=
ENST00000395227.2:c.366A>G ENSP00000378652.2:p.Leu122=
ENST00000425614.3:c.807A>G ENSP00000387640.2:p.Leu269=
ENST00000473881.2:c.*398A>G ENSP00000486667.1:n.*398A>G
NM_144701.2:c.1572A>G NP_653302.2:p.Leu524=
XM_005270516.2:c.810A>G XP_005270573.1:p.Leu270=
XM_011540789.1:c.1662A>G XP_011539091.1:p.Leu554=
XM_011540790.1:c.1572A>G XP_011539092.1:p.Leu524=
XM_011540791.1:c.1572A>G XP_011539093.1:p.Leu524=
XM_011540790.3:c.1572A>G XP_011539092.1:p.Leu524=
XM_011540791.3:c.1572A>G XP_011539093.1:p.Leu524=
XR_001736993.1:n.1652A>G
NM_144701.3:c.1572A>G MANE Select NP_653302.2:p.Leu524=