Canonical Allele Identifier: CA418438778

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724736G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259053G>A , CM000663.2:g.67259053G>A	GRCh38
NC_000001.10:g.67724736G>A , CM000663.1:g.67724736G>A	GRCh37
NC_000001.9:g.67497324G>A	NCBI36
NG_011498.1:g.97568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1654G>A	ENSP00000513138.1:n.1654G>A
ENST00000697150.1:c.1712G>A	ENSP00000513139.1:n.1712G>A
ENST00000697151.1:c.1645G>A	ENSP00000513140.1:n.1645G>A
ENST00000697164.1:c.1725G>A	ENSP00000513153.1:p.Leu575=
ENST00000697165.1:c.1512G>A	ENSP00000513154.1:p.Leu504=
ENST00000347310.10:c.1815G>A MANE Select	ENSP00000321345.5:p.Leu605=
ENST00000637002.1:c.1206G>A	ENSP00000490340.1:p.Leu402=
ENST00000347310.9:c.1815G>A	ENSP00000321345.5:p.Leu605=
ENST00000395227.2:c.609G>A	ENSP00000378652.2:p.Leu203=
ENST00000425614.3:c.1050G>A	ENSP00000387640.2:p.Leu350=
ENST00000473881.2:c.*641G>A	ENSP00000486667.1:n.*641G>A
NM_144701.2:c.1815G>A	NP_653302.2:p.Leu605=
XM_005270516.2:c.1053G>A	XP_005270573.1:p.Leu351=
XM_011540789.1:c.1905G>A	XP_011539091.1:p.Leu635=
XM_011540790.1:c.1815G>A	XP_011539092.1:p.Leu605=
XM_011540791.1:c.1815G>A	XP_011539093.1:p.Leu605=
XM_011540790.3:c.1815G>A	XP_011539092.1:p.Leu605=
XM_011540791.3:c.1815G>A	XP_011539093.1:p.Leu605=
XR_001736993.1:n.1895G>A
NM_144701.3:c.1815G>A MANE Select	NP_653302.2:p.Leu605=