Canonical Allele Identifier: CA340728592

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724425A>G (hg19) ; chr1:g.67258742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258742A>G , CM000663.2:g.67258742A>G	GRCh38
NC_000001.10:g.67724425A>G , CM000663.1:g.67724425A>G	GRCh37
NC_000001.9:g.67497013A>G	NCBI36
NG_011498.1:g.97257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1343A>G	ENSP00000513138.1:n.1343A>G
ENST00000697150.1:c.1401A>G	ENSP00000513139.1:n.1401A>G
ENST00000697151.1:c.1334A>G	ENSP00000513140.1:n.1334A>G
ENST00000697164.1:c.1414A>G	ENSP00000513153.1:p.Asn472Asp
ENST00000697165.1:c.1201A>G	ENSP00000513154.1:p.Asn401Asp
ENST00000347310.10:c.1504A>G MANE Select	ENSP00000321345.5:p.Asn502Asp
ENST00000637002.1:c.895A>G	ENSP00000490340.1:p.Asn299Asp
ENST00000347310.9:c.1504A>G	ENSP00000321345.5:p.Asn502Asp
ENST00000395227.2:c.298A>G	ENSP00000378652.2:p.Asn100Asp
ENST00000425614.3:c.739A>G	ENSP00000387640.2:p.Asn247Asp
ENST00000473881.2:c.*330A>G	ENSP00000486667.1:n.*330A>G
NM_144701.2:c.1504A>G	NP_653302.2:p.Asn502Asp
XM_005270516.2:c.742A>G	XP_005270573.1:p.Asn248Asp
XM_011540789.1:c.1594A>G	XP_011539091.1:p.Asn532Asp
XM_011540790.1:c.1504A>G	XP_011539092.1:p.Asn502Asp
XM_011540791.1:c.1504A>G	XP_011539093.1:p.Asn502Asp
XM_011540790.3:c.1504A>G	XP_011539092.1:p.Asn502Asp
XM_011540791.3:c.1504A>G	XP_011539093.1:p.Asn502Asp
XR_001736993.1:n.1584A>G
NM_144701.3:c.1504A>G MANE Select	NP_653302.2:p.Asn502Asp