Canonical Allele Identifier: CA340728985

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724560G>C (hg19) ; chr1:g.67258877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258877G>C , CM000663.2:g.67258877G>C	GRCh38
NC_000001.10:g.67724560G>C , CM000663.1:g.67724560G>C	GRCh37
NC_000001.9:g.67497148G>C	NCBI36
NG_011498.1:g.97392G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1478G>C	ENSP00000513138.1:n.1478G>C
ENST00000697150.1:c.1536G>C	ENSP00000513139.1:n.1536G>C
ENST00000697151.1:c.1469G>C	ENSP00000513140.1:n.1469G>C
ENST00000697164.1:c.1549G>C	ENSP00000513153.1:p.Gly517Arg
ENST00000697165.1:c.1336G>C	ENSP00000513154.1:p.Gly446Arg
ENST00000347310.10:c.1639G>C MANE Select	ENSP00000321345.5:p.Gly547Arg
ENST00000637002.1:c.1030G>C	ENSP00000490340.1:p.Gly344Arg
ENST00000347310.9:c.1639G>C	ENSP00000321345.5:p.Gly547Arg
ENST00000395227.2:c.433G>C	ENSP00000378652.2:p.Gly145Arg
ENST00000425614.3:c.874G>C	ENSP00000387640.2:p.Gly292Arg
ENST00000473881.2:c.*465G>C	ENSP00000486667.1:n.*465G>C
NM_144701.2:c.1639G>C	NP_653302.2:p.Gly547Arg
XM_005270516.2:c.877G>C	XP_005270573.1:p.Gly293Arg
XM_011540789.1:c.1729G>C	XP_011539091.1:p.Gly577Arg
XM_011540790.1:c.1639G>C	XP_011539092.1:p.Gly547Arg
XM_011540791.1:c.1639G>C	XP_011539093.1:p.Gly547Arg
XM_011540790.3:c.1639G>C	XP_011539092.1:p.Gly547Arg
XM_011540791.3:c.1639G>C	XP_011539093.1:p.Gly547Arg
XR_001736993.1:n.1719G>C
NM_144701.3:c.1639G>C MANE Select	NP_653302.2:p.Gly547Arg