Canonical Allele Identifier: CA418438582

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724580A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258897A>G , CM000663.2:g.67258897A>G	GRCh38
NC_000001.10:g.67724580A>G , CM000663.1:g.67724580A>G	GRCh37
NC_000001.9:g.67497168A>G	NCBI36
NG_011498.1:g.97412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1498A>G	ENSP00000513138.1:n.1498A>G
ENST00000697150.1:c.1556A>G	ENSP00000513139.1:n.1556A>G
ENST00000697151.1:c.1489A>G	ENSP00000513140.1:n.1489A>G
ENST00000697164.1:c.1569A>G	ENSP00000513153.1:p.Leu523=
ENST00000697165.1:c.1356A>G	ENSP00000513154.1:p.Leu452=
ENST00000347310.10:c.1659A>G MANE Select	ENSP00000321345.5:p.Leu553=
ENST00000637002.1:c.1050A>G	ENSP00000490340.1:p.Leu350=
ENST00000347310.9:c.1659A>G	ENSP00000321345.5:p.Leu553=
ENST00000395227.2:c.453A>G	ENSP00000378652.2:p.Leu151=
ENST00000425614.3:c.894A>G	ENSP00000387640.2:p.Leu298=
ENST00000473881.2:c.*485A>G	ENSP00000486667.1:n.*485A>G
NM_144701.2:c.1659A>G	NP_653302.2:p.Leu553=
XM_005270516.2:c.897A>G	XP_005270573.1:p.Leu299=
XM_011540789.1:c.1749A>G	XP_011539091.1:p.Leu583=
XM_011540790.1:c.1659A>G	XP_011539092.1:p.Leu553=
XM_011540791.1:c.1659A>G	XP_011539093.1:p.Leu553=
XM_011540790.3:c.1659A>G	XP_011539092.1:p.Leu553=
XM_011540791.3:c.1659A>G	XP_011539093.1:p.Leu553=
XR_001736993.1:n.1739A>G
NM_144701.3:c.1659A>G MANE Select	NP_653302.2:p.Leu553=