Canonical Allele Identifier: CA340729722

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724733G>T (hg19) ; chr1:g.67259050G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259050G>T , CM000663.2:g.67259050G>T	GRCh38
NC_000001.10:g.67724733G>T , CM000663.1:g.67724733G>T	GRCh37
NC_000001.9:g.67497321G>T	NCBI36
NG_011498.1:g.97565G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1651G>T	ENSP00000513138.1:n.1651G>T
ENST00000697150.1:c.1709G>T	ENSP00000513139.1:n.1709G>T
ENST00000697151.1:c.1642G>T	ENSP00000513140.1:n.1642G>T
ENST00000697164.1:c.1722G>T	ENSP00000513153.1:p.Glu574Asp
ENST00000697165.1:c.1509G>T	ENSP00000513154.1:p.Glu503Asp
ENST00000347310.10:c.1812G>T MANE Select	ENSP00000321345.5:p.Glu604Asp
ENST00000637002.1:c.1203G>T	ENSP00000490340.1:p.Glu401Asp
ENST00000347310.9:c.1812G>T	ENSP00000321345.5:p.Glu604Asp
ENST00000395227.2:c.606G>T	ENSP00000378652.2:p.Glu202Asp
ENST00000425614.3:c.1047G>T	ENSP00000387640.2:p.Glu349Asp
ENST00000473881.2:c.*638G>T	ENSP00000486667.1:n.*638G>T
NM_144701.2:c.1812G>T	NP_653302.2:p.Glu604Asp
XM_005270516.2:c.1050G>T	XP_005270573.1:p.Glu350Asp
XM_011540789.1:c.1902G>T	XP_011539091.1:p.Glu634Asp
XM_011540790.1:c.1812G>T	XP_011539092.1:p.Glu604Asp
XM_011540791.1:c.1812G>T	XP_011539093.1:p.Glu604Asp
XM_011540790.3:c.1812G>T	XP_011539092.1:p.Glu604Asp
XM_011540791.3:c.1812G>T	XP_011539093.1:p.Glu604Asp
XR_001736993.1:n.1892G>T
NM_144701.3:c.1812G>T MANE Select	NP_653302.2:p.Glu604Asp