Canonical Allele Identifier: CA340728590

Gene: IL23R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1343A>C	ENSP00000513138.1:n.1343A>C
ENST00000697150.1:c.1401A>C	ENSP00000513139.1:n.1401A>C
ENST00000697151.1:c.1334A>C	ENSP00000513140.1:n.1334A>C
ENST00000697164.1:c.1414A>C	ENSP00000513153.1:p.Asn472His
ENST00000697165.1:c.1201A>C	ENSP00000513154.1:p.Asn401His
ENST00000347310.10:c.1504A>C MANE Select	ENSP00000321345.5:p.Asn502His
ENST00000637002.1:c.895A>C	ENSP00000490340.1:p.Asn299His
ENST00000347310.9:c.1504A>C	ENSP00000321345.5:p.Asn502His
ENST00000395227.2:c.298A>C	ENSP00000378652.2:p.Asn100His
ENST00000425614.3:c.739A>C	ENSP00000387640.2:p.Asn247His
ENST00000473881.2:c.*330A>C	ENSP00000486667.1:n.*330A>C
NM_144701.2:c.1504A>C	NP_653302.2:p.Asn502His
XM_005270516.2:c.742A>C	XP_005270573.1:p.Asn248His
XM_011540789.1:c.1594A>C	XP_011539091.1:p.Asn532His
XM_011540790.1:c.1504A>C	XP_011539092.1:p.Asn502His
XM_011540791.1:c.1504A>C	XP_011539093.1:p.Asn502His
XM_011540790.3:c.1504A>C	XP_011539092.1:p.Asn502His
XM_011540791.3:c.1504A>C	XP_011539093.1:p.Asn502His
XR_001736993.1:n.1584A>C
NM_144701.3:c.1504A>C MANE Select	NP_653302.2:p.Asn502His