Canonical Allele Identifier: CA418438736

Gene: IL23R

Linked Data

• dbSNP Id: rs1233208238
• gnomAD v2: 1-67724700-A-G
• gnomAD v4: 1-67259017-A-G
• MyVariant Identifiers: chr1:g.67724700A>G (hg19) ; chr1:g.67259017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259017A>G , CM000663.2:g.67259017A>G	GRCh38
NC_000001.10:g.67724700A>G , CM000663.1:g.67724700A>G	GRCh37
NC_000001.9:g.67497288A>G	NCBI36
NG_011498.1:g.97532A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1618A>G	ENSP00000513138.1:n.1618A>G
ENST00000697150.1:c.1676A>G	ENSP00000513139.1:n.1676A>G
ENST00000697151.1:c.1609A>G	ENSP00000513140.1:n.1609A>G
ENST00000697164.1:c.1689A>G	ENSP00000513153.1:p.Glu563=
ENST00000697165.1:c.1476A>G	ENSP00000513154.1:p.Glu492=
ENST00000347310.10:c.1779A>G MANE Select	ENSP00000321345.5:p.Glu593=
ENST00000637002.1:c.1170A>G	ENSP00000490340.1:p.Glu390=
ENST00000347310.9:c.1779A>G	ENSP00000321345.5:p.Glu593=
ENST00000395227.2:c.573A>G	ENSP00000378652.2:p.Glu191=
ENST00000425614.3:c.1014A>G	ENSP00000387640.2:p.Glu338=
ENST00000473881.2:c.*605A>G	ENSP00000486667.1:n.*605A>G
NM_144701.2:c.1779A>G	NP_653302.2:p.Glu593=
XM_005270516.2:c.1017A>G	XP_005270573.1:p.Glu339=
XM_011540789.1:c.1869A>G	XP_011539091.1:p.Glu623=
XM_011540790.1:c.1779A>G	XP_011539092.1:p.Glu593=
XM_011540791.1:c.1779A>G	XP_011539093.1:p.Glu593=
XM_011540790.3:c.1779A>G	XP_011539092.1:p.Glu593=
XM_011540791.3:c.1779A>G	XP_011539093.1:p.Glu593=
XR_001736993.1:n.1859A>G
NM_144701.3:c.1779A>G MANE Select	NP_653302.2:p.Glu593=