Canonical Allele Identifier: CA340729969

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259097A>C , CM000663.2:g.67259097A>C	GRCh38
NC_000001.10:g.67724780A>C , CM000663.1:g.67724780A>C	GRCh37
NC_000001.9:g.67497368A>C	NCBI36
NG_011498.1:g.97612A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1859A>C MANE Select	NP_653302.2:p.His620Pro
ENST00000347310.10:c.1859A>C MANE Select	ENSP00000321345.5:p.His620Pro
NM_144701.2:c.1859A>C	NP_653302.2:p.His620Pro
ENST00000347310.9:c.1859A>C	ENSP00000321345.5:p.His620Pro
ENST00000395227.2:c.653A>C	ENSP00000378652.2:p.His218Pro
ENST00000425614.3:c.1094A>C	ENSP00000387640.2:p.His365Pro
ENST00000473881.2:c.*685A>C	ENSP00000486667.1:n.*685A>C
ENST00000637002.1:c.1250A>C	ENSP00000490340.1:p.His417Pro
ENST00000697149.1:c.1698A>C	ENSP00000513138.1:n.1698A>C
ENST00000697150.1:c.1756A>C	ENSP00000513139.1:n.1756A>C
ENST00000697151.1:c.1689A>C	ENSP00000513140.1:n.1689A>C
ENST00000697164.1:c.1769A>C	ENSP00000513153.1:p.His590Pro
ENST00000697165.1:c.1556A>C	ENSP00000513154.1:p.His519Pro
XM_005270516.2:c.1097A>C	XP_005270573.1:p.His366Pro
XM_011540789.1:c.1949A>C	XP_011539091.1:p.His650Pro
XM_011540790.1:c.1859A>C	XP_011539092.1:p.His620Pro
XM_011540790.3:c.1859A>C	XP_011539092.1:p.His620Pro
XM_011540791.1:c.1859A>C	XP_011539093.1:p.His620Pro
XM_011540791.3:c.1859A>C	XP_011539093.1:p.His620Pro
XR_001736993.1:n.1939A>C