Canonical Allele Identifier: CA340728707

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724476G>C (hg19) ; chr1:g.67258793G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258793G>C , CM000663.2:g.67258793G>C	GRCh38
NC_000001.10:g.67724476G>C , CM000663.1:g.67724476G>C	GRCh37
NC_000001.9:g.67497064G>C	NCBI36
NG_011498.1:g.97308G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1394G>C	ENSP00000513138.1:n.1394G>C
ENST00000697150.1:c.1452G>C	ENSP00000513139.1:n.1452G>C
ENST00000697151.1:c.1385G>C	ENSP00000513140.1:n.1385G>C
ENST00000697164.1:c.1465G>C	ENSP00000513153.1:p.Gly489Arg
ENST00000697165.1:c.1252G>C	ENSP00000513154.1:p.Gly418Arg
ENST00000347310.10:c.1555G>C MANE Select	ENSP00000321345.5:p.Gly519Arg
ENST00000637002.1:c.946G>C	ENSP00000490340.1:p.Gly316Arg
ENST00000347310.9:c.1555G>C	ENSP00000321345.5:p.Gly519Arg
ENST00000395227.2:c.349G>C	ENSP00000378652.2:p.Gly117Arg
ENST00000425614.3:c.790G>C	ENSP00000387640.2:p.Gly264Arg
ENST00000473881.2:c.*381G>C	ENSP00000486667.1:n.*381G>C
NM_144701.2:c.1555G>C	NP_653302.2:p.Gly519Arg
XM_005270516.2:c.793G>C	XP_005270573.1:p.Gly265Arg
XM_011540789.1:c.1645G>C	XP_011539091.1:p.Gly549Arg
XM_011540790.1:c.1555G>C	XP_011539092.1:p.Gly519Arg
XM_011540791.1:c.1555G>C	XP_011539093.1:p.Gly519Arg
XM_011540790.3:c.1555G>C	XP_011539092.1:p.Gly519Arg
XM_011540791.3:c.1555G>C	XP_011539093.1:p.Gly519Arg
XR_001736993.1:n.1635G>C
NM_144701.3:c.1555G>C MANE Select	NP_653302.2:p.Gly519Arg