Canonical Allele Identifier: CA340729323

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724626G>C (hg19) ; chr1:g.67258943G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258943G>C , CM000663.2:g.67258943G>C	GRCh38
NC_000001.10:g.67724626G>C , CM000663.1:g.67724626G>C	GRCh37
NC_000001.9:g.67497214G>C	NCBI36
NG_011498.1:g.97458G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1544G>C	ENSP00000513138.1:n.1544G>C
ENST00000697150.1:c.1602G>C	ENSP00000513139.1:n.1602G>C
ENST00000697151.1:c.1535G>C	ENSP00000513140.1:n.1535G>C
ENST00000697164.1:c.1615G>C	ENSP00000513153.1:p.Glu539Gln
ENST00000697165.1:c.1402G>C	ENSP00000513154.1:p.Glu468Gln
ENST00000347310.10:c.1705G>C MANE Select	ENSP00000321345.5:p.Glu569Gln
ENST00000637002.1:c.1096G>C	ENSP00000490340.1:p.Glu366Gln
ENST00000347310.9:c.1705G>C	ENSP00000321345.5:p.Glu569Gln
ENST00000395227.2:c.499G>C	ENSP00000378652.2:p.Glu167Gln
ENST00000425614.3:c.940G>C	ENSP00000387640.2:p.Glu314Gln
ENST00000473881.2:c.*531G>C	ENSP00000486667.1:n.*531G>C
NM_144701.2:c.1705G>C	NP_653302.2:p.Glu569Gln
XM_005270516.2:c.943G>C	XP_005270573.1:p.Glu315Gln
XM_011540789.1:c.1795G>C	XP_011539091.1:p.Glu599Gln
XM_011540790.1:c.1705G>C	XP_011539092.1:p.Glu569Gln
XM_011540791.1:c.1705G>C	XP_011539093.1:p.Glu569Gln
XM_011540790.3:c.1705G>C	XP_011539092.1:p.Glu569Gln
XM_011540791.3:c.1705G>C	XP_011539093.1:p.Glu569Gln
XR_001736993.1:n.1785G>C
NM_144701.3:c.1705G>C MANE Select	NP_653302.2:p.Glu569Gln