Canonical Allele Identifier: CA418438803

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724553A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258870A>T , CM000663.2:g.67258870A>T	GRCh38
NC_000001.10:g.67724553A>T , CM000663.1:g.67724553A>T	GRCh37
NC_000001.9:g.67497141A>T	NCBI36
NG_011498.1:g.97385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1471A>T	ENSP00000513138.1:n.1471A>T
ENST00000697150.1:c.1529A>T	ENSP00000513139.1:n.1529A>T
ENST00000697151.1:c.1462A>T	ENSP00000513140.1:n.1462A>T
ENST00000697164.1:c.1542A>T	ENSP00000513153.1:p.Ile514=
ENST00000697165.1:c.1329A>T	ENSP00000513154.1:p.Ile443=
ENST00000347310.10:c.1632A>T MANE Select	ENSP00000321345.5:p.Ile544=
ENST00000637002.1:c.1023A>T	ENSP00000490340.1:p.Ile341=
ENST00000347310.9:c.1632A>T	ENSP00000321345.5:p.Ile544=
ENST00000395227.2:c.426A>T	ENSP00000378652.2:p.Ile142=
ENST00000425614.3:c.867A>T	ENSP00000387640.2:p.Ile289=
ENST00000473881.2:c.*458A>T	ENSP00000486667.1:n.*458A>T
NM_144701.2:c.1632A>T	NP_653302.2:p.Ile544=
XM_005270516.2:c.870A>T	XP_005270573.1:p.Ile290=
XM_011540789.1:c.1722A>T	XP_011539091.1:p.Ile574=
XM_011540790.1:c.1632A>T	XP_011539092.1:p.Ile544=
XM_011540791.1:c.1632A>T	XP_011539093.1:p.Ile544=
XM_011540790.3:c.1632A>T	XP_011539092.1:p.Ile544=
XM_011540791.3:c.1632A>T	XP_011539093.1:p.Ile544=
XR_001736993.1:n.1712A>T
NM_144701.3:c.1632A>T MANE Select	NP_653302.2:p.Ile544=