Canonical Allele Identifier: CA340729305

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258940-G-C
• MyVariant Identifiers: chr1:g.67724623G>C (hg19) ; chr1:g.67258940G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258940G>C , CM000663.2:g.67258940G>C	GRCh38
NC_000001.10:g.67724623G>C , CM000663.1:g.67724623G>C	GRCh37
NC_000001.9:g.67497211G>C	NCBI36
NG_011498.1:g.97455G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1541G>C	ENSP00000513138.1:n.1541G>C
ENST00000697150.1:c.1599G>C	ENSP00000513139.1:n.1599G>C
ENST00000697151.1:c.1532G>C	ENSP00000513140.1:n.1532G>C
ENST00000697164.1:c.1612G>C	ENSP00000513153.1:p.Glu538Gln
ENST00000697165.1:c.1399G>C	ENSP00000513154.1:p.Glu467Gln
ENST00000347310.10:c.1702G>C MANE Select	ENSP00000321345.5:p.Glu568Gln
ENST00000637002.1:c.1093G>C	ENSP00000490340.1:p.Glu365Gln
ENST00000347310.9:c.1702G>C	ENSP00000321345.5:p.Glu568Gln
ENST00000395227.2:c.496G>C	ENSP00000378652.2:p.Glu166Gln
ENST00000425614.3:c.937G>C	ENSP00000387640.2:p.Glu313Gln
ENST00000473881.2:c.*528G>C	ENSP00000486667.1:n.*528G>C
NM_144701.2:c.1702G>C	NP_653302.2:p.Glu568Gln
XM_005270516.2:c.940G>C	XP_005270573.1:p.Glu314Gln
XM_011540789.1:c.1792G>C	XP_011539091.1:p.Glu598Gln
XM_011540790.1:c.1702G>C	XP_011539092.1:p.Glu568Gln
XM_011540791.1:c.1702G>C	XP_011539093.1:p.Glu568Gln
XM_011540790.3:c.1702G>C	XP_011539092.1:p.Glu568Gln
XM_011540791.3:c.1702G>C	XP_011539093.1:p.Glu568Gln
XR_001736993.1:n.1782G>C
NM_144701.3:c.1702G>C MANE Select	NP_653302.2:p.Glu568Gln