Canonical Allele Identifier: CA340730176

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724805A>C (hg19) ; chr1:g.67259122A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259122A>C , CM000663.2:g.67259122A>C	GRCh38
NC_000001.10:g.67724805A>C , CM000663.1:g.67724805A>C	GRCh37
NC_000001.9:g.67497393A>C	NCBI36
NG_011498.1:g.97637A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1723A>C	ENSP00000513138.1:n.1723A>C
ENST00000697150.1:c.1781A>C	ENSP00000513139.1:n.1781A>C
ENST00000697151.1:c.1714A>C	ENSP00000513140.1:n.1714A>C
ENST00000697164.1:c.1794A>C	ENSP00000513153.1:p.Glu598Asp
ENST00000697165.1:c.1581A>C	ENSP00000513154.1:p.Glu527Asp
ENST00000347310.10:c.1884A>C MANE Select	ENSP00000321345.5:p.Glu628Asp
ENST00000637002.1:c.1275A>C	ENSP00000490340.1:p.Glu425Asp
ENST00000347310.9:c.1884A>C	ENSP00000321345.5:p.Glu628Asp
ENST00000395227.2:c.678A>C	ENSP00000378652.2:p.Glu226Asp
ENST00000425614.3:c.1119A>C	ENSP00000387640.2:p.Glu373Asp
ENST00000473881.2:c.*710A>C	ENSP00000486667.1:n.*710A>C
NM_144701.2:c.1884A>C	NP_653302.2:p.Glu628Asp
XM_005270516.2:c.1122A>C	XP_005270573.1:p.Glu374Asp
XM_011540789.1:c.1974A>C	XP_011539091.1:p.Glu658Asp
XM_011540790.1:c.1884A>C	XP_011539092.1:p.Glu628Asp
XM_011540791.1:c.1884A>C	XP_011539093.1:p.Glu628Asp
XM_011540790.3:c.1884A>C	XP_011539092.1:p.Glu628Asp
XM_011540791.3:c.1884A>C	XP_011539093.1:p.Glu628Asp
XR_001736993.1:n.1964A>C
NM_144701.3:c.1884A>C MANE Select	NP_653302.2:p.Glu628Asp