Canonical Allele Identifier: CA340728684

Gene: IL23R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1383C>G	ENSP00000513138.1:n.1383C>G
ENST00000697150.1:c.1441C>G	ENSP00000513139.1:n.1441C>G
ENST00000697151.1:c.1374C>G	ENSP00000513140.1:n.1374C>G
ENST00000697164.1:c.1454C>G	ENSP00000513153.1:p.Ser485Cys
ENST00000697165.1:c.1241C>G	ENSP00000513154.1:p.Ser414Cys
ENST00000347310.10:c.1544C>G MANE Select	ENSP00000321345.5:p.Ser515Cys
ENST00000637002.1:c.935C>G	ENSP00000490340.1:p.Ser312Cys
ENST00000347310.9:c.1544C>G	ENSP00000321345.5:p.Ser515Cys
ENST00000395227.2:c.338C>G	ENSP00000378652.2:p.Ser113Cys
ENST00000425614.3:c.779C>G	ENSP00000387640.2:p.Ser260Cys
ENST00000473881.2:c.*370C>G	ENSP00000486667.1:n.*370C>G
NM_144701.2:c.1544C>G	NP_653302.2:p.Ser515Cys
XM_005270516.2:c.782C>G	XP_005270573.1:p.Ser261Cys
XM_011540789.1:c.1634C>G	XP_011539091.1:p.Ser545Cys
XM_011540790.1:c.1544C>G	XP_011539092.1:p.Ser515Cys
XM_011540791.1:c.1544C>G	XP_011539093.1:p.Ser515Cys
XM_011540790.3:c.1544C>G	XP_011539092.1:p.Ser515Cys
XM_011540791.3:c.1544C>G	XP_011539093.1:p.Ser515Cys
XR_001736993.1:n.1624C>G
NM_144701.3:c.1544C>G MANE Select	NP_653302.2:p.Ser515Cys