Canonical Allele Identifier: CA340729820

Gene: IL23R

Linked Data

• dbSNP Id: rs1189559735
• gnomAD v2: 1-67724754-T-A
• gnomAD v4: 1-67259071-T-A
• MyVariant Identifiers: chr1:g.67724754T>A (hg19) ; chr1:g.67259071T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259071T>A , CM000663.2:g.67259071T>A	GRCh38
NC_000001.10:g.67724754T>A , CM000663.1:g.67724754T>A	GRCh37
NC_000001.9:g.67497342T>A	NCBI36
NG_011498.1:g.97586T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1672T>A	ENSP00000513138.1:n.1672T>A
ENST00000697150.1:c.1730T>A	ENSP00000513139.1:n.1730T>A
ENST00000697151.1:c.1663T>A	ENSP00000513140.1:n.1663T>A
ENST00000697164.1:c.1743T>A	ENSP00000513153.1:p.Tyr581Ter
ENST00000697165.1:c.1530T>A	ENSP00000513154.1:p.Tyr510Ter
ENST00000347310.10:c.1833T>A MANE Select	ENSP00000321345.5:p.Tyr611Ter
ENST00000637002.1:c.1224T>A	ENSP00000490340.1:p.Tyr408Ter
ENST00000347310.9:c.1833T>A	ENSP00000321345.5:p.Tyr611Ter
ENST00000395227.2:c.627T>A	ENSP00000378652.2:p.Tyr209Ter
ENST00000425614.3:c.1068T>A	ENSP00000387640.2:p.Tyr356Ter
ENST00000473881.2:c.*659T>A	ENSP00000486667.1:n.*659T>A
NM_144701.2:c.1833T>A	NP_653302.2:p.Tyr611Ter
XM_005270516.2:c.1071T>A	XP_005270573.1:p.Tyr357Ter
XM_011540789.1:c.1923T>A	XP_011539091.1:p.Tyr641Ter
XM_011540790.1:c.1833T>A	XP_011539092.1:p.Tyr611Ter
XM_011540791.1:c.1833T>A	XP_011539093.1:p.Tyr611Ter
XM_011540790.3:c.1833T>A	XP_011539092.1:p.Tyr611Ter
XM_011540791.3:c.1833T>A	XP_011539093.1:p.Tyr611Ter
XR_001736993.1:n.1913T>A
NM_144701.3:c.1833T>A MANE Select	NP_653302.2:p.Tyr611Ter