Canonical Allele Identifier: CA340730058

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724789G>C (hg19) ; chr1:g.67259106G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259106G>C , CM000663.2:g.67259106G>C	GRCh38
NC_000001.10:g.67724789G>C , CM000663.1:g.67724789G>C	GRCh37
NC_000001.9:g.67497377G>C	NCBI36
NG_011498.1:g.97621G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1707G>C	ENSP00000513138.1:n.1707G>C
ENST00000697150.1:c.1765G>C	ENSP00000513139.1:n.1765G>C
ENST00000697151.1:c.1698G>C	ENSP00000513140.1:n.1698G>C
ENST00000697164.1:c.1778G>C	ENSP00000513153.1:p.Arg593Thr
ENST00000697165.1:c.1565G>C	ENSP00000513154.1:p.Arg522Thr
ENST00000347310.10:c.1868G>C MANE Select	ENSP00000321345.5:p.Arg623Thr
ENST00000637002.1:c.1259G>C	ENSP00000490340.1:p.Arg420Thr
ENST00000347310.9:c.1868G>C	ENSP00000321345.5:p.Arg623Thr
ENST00000395227.2:c.662G>C	ENSP00000378652.2:p.Arg221Thr
ENST00000425614.3:c.1103G>C	ENSP00000387640.2:p.Arg368Thr
ENST00000473881.2:c.*694G>C	ENSP00000486667.1:n.*694G>C
NM_144701.2:c.1868G>C	NP_653302.2:p.Arg623Thr
XM_005270516.2:c.1106G>C	XP_005270573.1:p.Arg369Thr
XM_011540789.1:c.1958G>C	XP_011539091.1:p.Arg653Thr
XM_011540790.1:c.1868G>C	XP_011539092.1:p.Arg623Thr
XM_011540791.1:c.1868G>C	XP_011539093.1:p.Arg623Thr
XM_011540790.3:c.1868G>C	XP_011539092.1:p.Arg623Thr
XM_011540791.3:c.1868G>C	XP_011539093.1:p.Arg623Thr
XR_001736993.1:n.1948G>C
NM_144701.3:c.1868G>C MANE Select	NP_653302.2:p.Arg623Thr