Canonical Allele Identifier: CA340728845

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724531T>G (hg19) ; chr1:g.67258848T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258848T>G , CM000663.2:g.67258848T>G	GRCh38
NC_000001.10:g.67724531T>G , CM000663.1:g.67724531T>G	GRCh37
NC_000001.9:g.67497119T>G	NCBI36
NG_011498.1:g.97363T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1449T>G	ENSP00000513138.1:n.1449T>G
ENST00000697150.1:c.1507T>G	ENSP00000513139.1:n.1507T>G
ENST00000697151.1:c.1440T>G	ENSP00000513140.1:n.1440T>G
ENST00000697164.1:c.1520T>G	ENSP00000513153.1:p.Val507Gly
ENST00000697165.1:c.1307T>G	ENSP00000513154.1:p.Val436Gly
ENST00000347310.10:c.1610T>G MANE Select	ENSP00000321345.5:p.Val537Gly
ENST00000637002.1:c.1001T>G	ENSP00000490340.1:p.Val334Gly
ENST00000347310.9:c.1610T>G	ENSP00000321345.5:p.Val537Gly
ENST00000395227.2:c.404T>G	ENSP00000378652.2:p.Val135Gly
ENST00000425614.3:c.845T>G	ENSP00000387640.2:p.Val282Gly
ENST00000473881.2:c.*436T>G	ENSP00000486667.1:n.*436T>G
NM_144701.2:c.1610T>G	NP_653302.2:p.Val537Gly
XM_005270516.2:c.848T>G	XP_005270573.1:p.Val283Gly
XM_011540789.1:c.1700T>G	XP_011539091.1:p.Val567Gly
XM_011540790.1:c.1610T>G	XP_011539092.1:p.Val537Gly
XM_011540791.1:c.1610T>G	XP_011539093.1:p.Val537Gly
XM_011540790.3:c.1610T>G	XP_011539092.1:p.Val537Gly
XM_011540791.3:c.1610T>G	XP_011539093.1:p.Val537Gly
XR_001736993.1:n.1690T>G
NM_144701.3:c.1610T>G MANE Select	NP_653302.2:p.Val537Gly