Canonical Allele Identifier: CA418438728

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258807-G-A
• MyVariant Identifiers: chr1:g.67724490G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258807G>A , CM000663.2:g.67258807G>A	GRCh38
NC_000001.10:g.67724490G>A , CM000663.1:g.67724490G>A	GRCh37
NC_000001.9:g.67497078G>A	NCBI36
NG_011498.1:g.97322G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1408G>A	ENSP00000513138.1:n.1408G>A
ENST00000697150.1:c.1466G>A	ENSP00000513139.1:n.1466G>A
ENST00000697151.1:c.1399G>A	ENSP00000513140.1:n.1399G>A
ENST00000697164.1:c.1479G>A	ENSP00000513153.1:p.Arg493=
ENST00000697165.1:c.1266G>A	ENSP00000513154.1:p.Arg422=
ENST00000347310.10:c.1569G>A MANE Select	ENSP00000321345.5:p.Arg523=
ENST00000637002.1:c.960G>A	ENSP00000490340.1:p.Arg320=
ENST00000347310.9:c.1569G>A	ENSP00000321345.5:p.Arg523=
ENST00000395227.2:c.363G>A	ENSP00000378652.2:p.Arg121=
ENST00000425614.3:c.804G>A	ENSP00000387640.2:p.Arg268=
ENST00000473881.2:c.*395G>A	ENSP00000486667.1:n.*395G>A
NM_144701.2:c.1569G>A	NP_653302.2:p.Arg523=
XM_005270516.2:c.807G>A	XP_005270573.1:p.Arg269=
XM_011540789.1:c.1659G>A	XP_011539091.1:p.Arg553=
XM_011540790.1:c.1569G>A	XP_011539092.1:p.Arg523=
XM_011540791.1:c.1569G>A	XP_011539093.1:p.Arg523=
XM_011540790.3:c.1569G>A	XP_011539092.1:p.Arg523=
XM_011540791.3:c.1569G>A	XP_011539093.1:p.Arg523=
XR_001736993.1:n.1649G>A
NM_144701.3:c.1569G>A MANE Select	NP_653302.2:p.Arg523=