Canonical Allele Identifier: CA340728719

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724482A>G (hg19) ; chr1:g.67258799A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258799A>G , CM000663.2:g.67258799A>G	GRCh38
NC_000001.10:g.67724482A>G , CM000663.1:g.67724482A>G	GRCh37
NC_000001.9:g.67497070A>G	NCBI36
NG_011498.1:g.97314A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1400A>G	ENSP00000513138.1:n.1400A>G
ENST00000697150.1:c.1458A>G	ENSP00000513139.1:n.1458A>G
ENST00000697151.1:c.1391A>G	ENSP00000513140.1:n.1391A>G
ENST00000697164.1:c.1471A>G	ENSP00000513153.1:p.Asn491Asp
ENST00000697165.1:c.1258A>G	ENSP00000513154.1:p.Asn420Asp
ENST00000347310.10:c.1561A>G MANE Select	ENSP00000321345.5:p.Asn521Asp
ENST00000637002.1:c.952A>G	ENSP00000490340.1:p.Asn318Asp
ENST00000347310.9:c.1561A>G	ENSP00000321345.5:p.Asn521Asp
ENST00000395227.2:c.355A>G	ENSP00000378652.2:p.Asn119Asp
ENST00000425614.3:c.796A>G	ENSP00000387640.2:p.Asn266Asp
ENST00000473881.2:c.*387A>G	ENSP00000486667.1:n.*387A>G
NM_144701.2:c.1561A>G	NP_653302.2:p.Asn521Asp
XM_005270516.2:c.799A>G	XP_005270573.1:p.Asn267Asp
XM_011540789.1:c.1651A>G	XP_011539091.1:p.Asn551Asp
XM_011540790.1:c.1561A>G	XP_011539092.1:p.Asn521Asp
XM_011540791.1:c.1561A>G	XP_011539093.1:p.Asn521Asp
XM_011540790.3:c.1561A>G	XP_011539092.1:p.Asn521Asp
XM_011540791.3:c.1561A>G	XP_011539093.1:p.Asn521Asp
XR_001736993.1:n.1641A>G
NM_144701.3:c.1561A>G MANE Select	NP_653302.2:p.Asn521Asp