Canonical Allele Identifier: CA418438592

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724589A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258906A>T , CM000663.2:g.67258906A>T	GRCh38
NC_000001.10:g.67724589A>T , CM000663.1:g.67724589A>T	GRCh37
NC_000001.9:g.67497177A>T	NCBI36
NG_011498.1:g.97421A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1507A>T	ENSP00000513138.1:n.1507A>T
ENST00000697150.1:c.1565A>T	ENSP00000513139.1:n.1565A>T
ENST00000697151.1:c.1498A>T	ENSP00000513140.1:n.1498A>T
ENST00000697164.1:c.1578A>T	ENSP00000513153.1:p.Gly526=
ENST00000697165.1:c.1365A>T	ENSP00000513154.1:p.Gly455=
ENST00000347310.10:c.1668A>T MANE Select	ENSP00000321345.5:p.Gly556=
ENST00000637002.1:c.1059A>T	ENSP00000490340.1:p.Gly353=
ENST00000347310.9:c.1668A>T	ENSP00000321345.5:p.Gly556=
ENST00000395227.2:c.462A>T	ENSP00000378652.2:p.Gly154=
ENST00000425614.3:c.903A>T	ENSP00000387640.2:p.Gly301=
ENST00000473881.2:c.*494A>T	ENSP00000486667.1:n.*494A>T
NM_144701.2:c.1668A>T	NP_653302.2:p.Gly556=
XM_005270516.2:c.906A>T	XP_005270573.1:p.Gly302=
XM_011540789.1:c.1758A>T	XP_011539091.1:p.Gly586=
XM_011540790.1:c.1668A>T	XP_011539092.1:p.Gly556=
XM_011540791.1:c.1668A>T	XP_011539093.1:p.Gly556=
XM_011540790.3:c.1668A>T	XP_011539092.1:p.Gly556=
XM_011540791.3:c.1668A>T	XP_011539093.1:p.Gly556=
XR_001736993.1:n.1748A>T
NM_144701.3:c.1668A>T MANE Select	NP_653302.2:p.Gly556=