Canonical Allele Identifier: CA340729580

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724696A>G (hg19) ; chr1:g.67259013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259013A>G , CM000663.2:g.67259013A>G	GRCh38
NC_000001.10:g.67724696A>G , CM000663.1:g.67724696A>G	GRCh37
NC_000001.9:g.67497284A>G	NCBI36
NG_011498.1:g.97528A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1614A>G	ENSP00000513138.1:n.1614A>G
ENST00000697150.1:c.1672A>G	ENSP00000513139.1:n.1672A>G
ENST00000697151.1:c.1605A>G	ENSP00000513140.1:n.1605A>G
ENST00000697164.1:c.1685A>G	ENSP00000513153.1:p.Asp562Gly
ENST00000697165.1:c.1472A>G	ENSP00000513154.1:p.Asp491Gly
ENST00000347310.10:c.1775A>G MANE Select	ENSP00000321345.5:p.Asp592Gly
ENST00000637002.1:c.1166A>G	ENSP00000490340.1:p.Asp389Gly
ENST00000347310.9:c.1775A>G	ENSP00000321345.5:p.Asp592Gly
ENST00000395227.2:c.569A>G	ENSP00000378652.2:p.Asp190Gly
ENST00000425614.3:c.1010A>G	ENSP00000387640.2:p.Asp337Gly
ENST00000473881.2:c.*601A>G	ENSP00000486667.1:n.*601A>G
NM_144701.2:c.1775A>G	NP_653302.2:p.Asp592Gly
XM_005270516.2:c.1013A>G	XP_005270573.1:p.Asp338Gly
XM_011540789.1:c.1865A>G	XP_011539091.1:p.Asp622Gly
XM_011540790.1:c.1775A>G	XP_011539092.1:p.Asp592Gly
XM_011540791.1:c.1775A>G	XP_011539093.1:p.Asp592Gly
XM_011540790.3:c.1775A>G	XP_011539092.1:p.Asp592Gly
XM_011540791.3:c.1775A>G	XP_011539093.1:p.Asp592Gly
XR_001736993.1:n.1855A>G
NM_144701.3:c.1775A>G MANE Select	NP_653302.2:p.Asp592Gly