Canonical Allele Identifier: CA340729168

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258908-A-C
• MyVariant Identifiers: chr1:g.67724591A>C (hg19) ; chr1:g.67258908A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258908A>C , CM000663.2:g.67258908A>C	GRCh38
NC_000001.10:g.67724591A>C , CM000663.1:g.67724591A>C	GRCh37
NC_000001.9:g.67497179A>C	NCBI36
NG_011498.1:g.97423A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1509A>C	ENSP00000513138.1:n.1509A>C
ENST00000697150.1:c.1567A>C	ENSP00000513139.1:n.1567A>C
ENST00000697151.1:c.1500A>C	ENSP00000513140.1:n.1500A>C
ENST00000697164.1:c.1580A>C	ENSP00000513153.1:p.Glu527Ala
ENST00000697165.1:c.1367A>C	ENSP00000513154.1:p.Glu456Ala
ENST00000347310.10:c.1670A>C MANE Select	ENSP00000321345.5:p.Glu557Ala
ENST00000637002.1:c.1061A>C	ENSP00000490340.1:p.Glu354Ala
ENST00000347310.9:c.1670A>C	ENSP00000321345.5:p.Glu557Ala
ENST00000395227.2:c.464A>C	ENSP00000378652.2:p.Glu155Ala
ENST00000425614.3:c.905A>C	ENSP00000387640.2:p.Glu302Ala
ENST00000473881.2:c.*496A>C	ENSP00000486667.1:n.*496A>C
NM_144701.2:c.1670A>C	NP_653302.2:p.Glu557Ala
XM_005270516.2:c.908A>C	XP_005270573.1:p.Glu303Ala
XM_011540789.1:c.1760A>C	XP_011539091.1:p.Glu587Ala
XM_011540790.1:c.1670A>C	XP_011539092.1:p.Glu557Ala
XM_011540791.1:c.1670A>C	XP_011539093.1:p.Glu557Ala
XM_011540790.3:c.1670A>C	XP_011539092.1:p.Glu557Ala
XM_011540791.3:c.1670A>C	XP_011539093.1:p.Glu557Ala
XR_001736993.1:n.1750A>C
NM_144701.3:c.1670A>C MANE Select	NP_653302.2:p.Glu557Ala