Canonical Allele Identifier: CA418438821

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724772G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259089G>A , CM000663.2:g.67259089G>A	GRCh38
NC_000001.10:g.67724772G>A , CM000663.1:g.67724772G>A	GRCh37
NC_000001.9:g.67497360G>A	NCBI36
NG_011498.1:g.97604G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1690G>A	ENSP00000513138.1:n.1690G>A
ENST00000697150.1:c.1748G>A	ENSP00000513139.1:n.1748G>A
ENST00000697151.1:c.1681G>A	ENSP00000513140.1:n.1681G>A
ENST00000697164.1:c.1761G>A	ENSP00000513153.1:p.Leu587=
ENST00000697165.1:c.1548G>A	ENSP00000513154.1:p.Leu516=
ENST00000347310.10:c.1851G>A MANE Select	ENSP00000321345.5:p.Leu617=
ENST00000637002.1:c.1242G>A	ENSP00000490340.1:p.Leu414=
ENST00000347310.9:c.1851G>A	ENSP00000321345.5:p.Leu617=
ENST00000395227.2:c.645G>A	ENSP00000378652.2:p.Leu215=
ENST00000425614.3:c.1086G>A	ENSP00000387640.2:p.Leu362=
ENST00000473881.2:c.*677G>A	ENSP00000486667.1:n.*677G>A
NM_144701.2:c.1851G>A	NP_653302.2:p.Leu617=
XM_005270516.2:c.1089G>A	XP_005270573.1:p.Leu363=
XM_011540789.1:c.1941G>A	XP_011539091.1:p.Leu647=
XM_011540790.1:c.1851G>A	XP_011539092.1:p.Leu617=
XM_011540791.1:c.1851G>A	XP_011539093.1:p.Leu617=
XM_011540790.3:c.1851G>A	XP_011539092.1:p.Leu617=
XM_011540791.3:c.1851G>A	XP_011539093.1:p.Leu617=
XR_001736993.1:n.1931G>A
NM_144701.3:c.1851G>A MANE Select	NP_653302.2:p.Leu617=