Canonical Allele Identifier: CA340729711

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724731G>C (hg19) ; chr1:g.67259048G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259048G>C , CM000663.2:g.67259048G>C	GRCh38
NC_000001.10:g.67724731G>C , CM000663.1:g.67724731G>C	GRCh37
NC_000001.9:g.67497319G>C	NCBI36
NG_011498.1:g.97563G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1649G>C	ENSP00000513138.1:n.1649G>C
ENST00000697150.1:c.1707G>C	ENSP00000513139.1:n.1707G>C
ENST00000697151.1:c.1640G>C	ENSP00000513140.1:n.1640G>C
ENST00000697164.1:c.1720G>C	ENSP00000513153.1:p.Glu574Gln
ENST00000697165.1:c.1507G>C	ENSP00000513154.1:p.Glu503Gln
ENST00000347310.10:c.1810G>C MANE Select	ENSP00000321345.5:p.Glu604Gln
ENST00000637002.1:c.1201G>C	ENSP00000490340.1:p.Glu401Gln
ENST00000347310.9:c.1810G>C	ENSP00000321345.5:p.Glu604Gln
ENST00000395227.2:c.604G>C	ENSP00000378652.2:p.Glu202Gln
ENST00000425614.3:c.1045G>C	ENSP00000387640.2:p.Glu349Gln
ENST00000473881.2:c.*636G>C	ENSP00000486667.1:n.*636G>C
NM_144701.2:c.1810G>C	NP_653302.2:p.Glu604Gln
XM_005270516.2:c.1048G>C	XP_005270573.1:p.Glu350Gln
XM_011540789.1:c.1900G>C	XP_011539091.1:p.Glu634Gln
XM_011540790.1:c.1810G>C	XP_011539092.1:p.Glu604Gln
XM_011540791.1:c.1810G>C	XP_011539093.1:p.Glu604Gln
XM_011540790.3:c.1810G>C	XP_011539092.1:p.Glu604Gln
XM_011540791.3:c.1810G>C	XP_011539093.1:p.Glu604Gln
XR_001736993.1:n.1890G>C
NM_144701.3:c.1810G>C MANE Select	NP_653302.2:p.Glu604Gln