Canonical Allele Identifier: CA340728683

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724465C>A (hg19) ; chr1:g.67258782C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258782C>A , CM000663.2:g.67258782C>A	GRCh38
NC_000001.10:g.67724465C>A , CM000663.1:g.67724465C>A	GRCh37
NC_000001.9:g.67497053C>A	NCBI36
NG_011498.1:g.97297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1383C>A	ENSP00000513138.1:n.1383C>A
ENST00000697150.1:c.1441C>A	ENSP00000513139.1:n.1441C>A
ENST00000697151.1:c.1374C>A	ENSP00000513140.1:n.1374C>A
ENST00000697164.1:c.1454C>A	ENSP00000513153.1:p.Ser485Tyr
ENST00000697165.1:c.1241C>A	ENSP00000513154.1:p.Ser414Tyr
ENST00000347310.10:c.1544C>A MANE Select	ENSP00000321345.5:p.Ser515Tyr
ENST00000637002.1:c.935C>A	ENSP00000490340.1:p.Ser312Tyr
ENST00000347310.9:c.1544C>A	ENSP00000321345.5:p.Ser515Tyr
ENST00000395227.2:c.338C>A	ENSP00000378652.2:p.Ser113Tyr
ENST00000425614.3:c.779C>A	ENSP00000387640.2:p.Ser260Tyr
ENST00000473881.2:c.*370C>A	ENSP00000486667.1:n.*370C>A
NM_144701.2:c.1544C>A	NP_653302.2:p.Ser515Tyr
XM_005270516.2:c.782C>A	XP_005270573.1:p.Ser261Tyr
XM_011540789.1:c.1634C>A	XP_011539091.1:p.Ser545Tyr
XM_011540790.1:c.1544C>A	XP_011539092.1:p.Ser515Tyr
XM_011540791.1:c.1544C>A	XP_011539093.1:p.Ser515Tyr
XM_011540790.3:c.1544C>A	XP_011539092.1:p.Ser515Tyr
XM_011540791.3:c.1544C>A	XP_011539093.1:p.Ser515Tyr
XR_001736993.1:n.1624C>A
NM_144701.3:c.1544C>A MANE Select	NP_653302.2:p.Ser515Tyr