Canonical Allele Identifier: CA340729527

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724680C>G (hg19) ; chr1:g.67258997C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258997C>G , CM000663.2:g.67258997C>G	GRCh38
NC_000001.10:g.67724680C>G , CM000663.1:g.67724680C>G	GRCh37
NC_000001.9:g.67497268C>G	NCBI36
NG_011498.1:g.97512C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1598C>G	ENSP00000513138.1:n.1598C>G
ENST00000697150.1:c.1656C>G	ENSP00000513139.1:n.1656C>G
ENST00000697151.1:c.1589C>G	ENSP00000513140.1:n.1589C>G
ENST00000697164.1:c.1669C>G	ENSP00000513153.1:p.Gln557Glu
ENST00000697165.1:c.1456C>G	ENSP00000513154.1:p.Gln486Glu
ENST00000347310.10:c.1759C>G MANE Select	ENSP00000321345.5:p.Gln587Glu
ENST00000637002.1:c.1150C>G	ENSP00000490340.1:p.Gln384Glu
ENST00000347310.9:c.1759C>G	ENSP00000321345.5:p.Gln587Glu
ENST00000395227.2:c.553C>G	ENSP00000378652.2:p.Gln185Glu
ENST00000425614.3:c.994C>G	ENSP00000387640.2:p.Gln332Glu
ENST00000473881.2:c.*585C>G	ENSP00000486667.1:n.*585C>G
NM_144701.2:c.1759C>G	NP_653302.2:p.Gln587Glu
XM_005270516.2:c.997C>G	XP_005270573.1:p.Gln333Glu
XM_011540789.1:c.1849C>G	XP_011539091.1:p.Gln617Glu
XM_011540790.1:c.1759C>G	XP_011539092.1:p.Gln587Glu
XM_011540791.1:c.1759C>G	XP_011539093.1:p.Gln587Glu
XM_011540790.3:c.1759C>G	XP_011539092.1:p.Gln587Glu
XM_011540791.3:c.1759C>G	XP_011539093.1:p.Gln587Glu
XR_001736993.1:n.1839C>G
NM_144701.3:c.1759C>G MANE Select	NP_653302.2:p.Gln587Glu