Canonical Allele Identifier: CA418438752

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724715G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259032G>A , CM000663.2:g.67259032G>A	GRCh38
NC_000001.10:g.67724715G>A , CM000663.1:g.67724715G>A	GRCh37
NC_000001.9:g.67497303G>A	NCBI36
NG_011498.1:g.97547G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1633G>A	ENSP00000513138.1:n.1633G>A
ENST00000697150.1:c.1691G>A	ENSP00000513139.1:n.1691G>A
ENST00000697151.1:c.1624G>A	ENSP00000513140.1:n.1624G>A
ENST00000697164.1:c.1704G>A	ENSP00000513153.1:p.Leu568=
ENST00000697165.1:c.1491G>A	ENSP00000513154.1:p.Leu497=
ENST00000347310.10:c.1794G>A MANE Select	ENSP00000321345.5:p.Leu598=
ENST00000637002.1:c.1185G>A	ENSP00000490340.1:p.Leu395=
ENST00000347310.9:c.1794G>A	ENSP00000321345.5:p.Leu598=
ENST00000395227.2:c.588G>A	ENSP00000378652.2:p.Leu196=
ENST00000425614.3:c.1029G>A	ENSP00000387640.2:p.Leu343=
ENST00000473881.2:c.*620G>A	ENSP00000486667.1:n.*620G>A
NM_144701.2:c.1794G>A	NP_653302.2:p.Leu598=
XM_005270516.2:c.1032G>A	XP_005270573.1:p.Leu344=
XM_011540789.1:c.1884G>A	XP_011539091.1:p.Leu628=
XM_011540790.1:c.1794G>A	XP_011539092.1:p.Leu598=
XM_011540791.1:c.1794G>A	XP_011539093.1:p.Leu598=
XM_011540790.3:c.1794G>A	XP_011539092.1:p.Leu598=
XM_011540791.3:c.1794G>A	XP_011539093.1:p.Leu598=
XR_001736993.1:n.1874G>A
NM_144701.3:c.1794G>A MANE Select	NP_653302.2:p.Leu598=