Canonical Allele Identifier: CA340728512

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724412T>G (hg19) ; chr1:g.67258729T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258729T>G , CM000663.2:g.67258729T>G	GRCh38
NC_000001.10:g.67724412T>G , CM000663.1:g.67724412T>G	GRCh37
NC_000001.9:g.67497000T>G	NCBI36
NG_011498.1:g.97244T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1330T>G	ENSP00000513138.1:n.1330T>G
ENST00000697150.1:c.1388T>G	ENSP00000513139.1:n.1388T>G
ENST00000697151.1:c.1321T>G	ENSP00000513140.1:n.1321T>G
ENST00000697164.1:c.1401T>G	ENSP00000513153.1:p.His467Gln
ENST00000697165.1:c.1188T>G	ENSP00000513154.1:p.His396Gln
ENST00000347310.10:c.1491T>G MANE Select	ENSP00000321345.5:p.His497Gln
ENST00000637002.1:c.882T>G	ENSP00000490340.1:p.His294Gln
ENST00000347310.9:c.1491T>G	ENSP00000321345.5:p.His497Gln
ENST00000395227.2:c.285T>G	ENSP00000378652.2:p.His95Gln
ENST00000425614.3:c.726T>G	ENSP00000387640.2:p.His242Gln
ENST00000473881.2:c.*317T>G	ENSP00000486667.1:n.*317T>G
NM_144701.2:c.1491T>G	NP_653302.2:p.His497Gln
XM_005270516.2:c.729T>G	XP_005270573.1:p.His243Gln
XM_011540789.1:c.1581T>G	XP_011539091.1:p.His527Gln
XM_011540790.1:c.1491T>G	XP_011539092.1:p.His497Gln
XM_011540791.1:c.1491T>G	XP_011539093.1:p.His497Gln
XM_011540790.3:c.1491T>G	XP_011539092.1:p.His497Gln
XM_011540791.3:c.1491T>G	XP_011539093.1:p.His497Gln
XR_001736993.1:n.1571T>G
NM_144701.3:c.1491T>G MANE Select	NP_653302.2:p.His497Gln