Canonical Allele Identifier: CA340729363

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724635A>G (hg19) ; chr1:g.67258952A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258952A>G , CM000663.2:g.67258952A>G	GRCh38
NC_000001.10:g.67724635A>G , CM000663.1:g.67724635A>G	GRCh37
NC_000001.9:g.67497223A>G	NCBI36
NG_011498.1:g.97467A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1553A>G	ENSP00000513138.1:n.1553A>G
ENST00000697150.1:c.1611A>G	ENSP00000513139.1:n.1611A>G
ENST00000697151.1:c.1544A>G	ENSP00000513140.1:n.1544A>G
ENST00000697164.1:c.1624A>G	ENSP00000513153.1:p.Thr542Ala
ENST00000697165.1:c.1411A>G	ENSP00000513154.1:p.Thr471Ala
ENST00000347310.10:c.1714A>G MANE Select	ENSP00000321345.5:p.Thr572Ala
ENST00000637002.1:c.1105A>G	ENSP00000490340.1:p.Thr369Ala
ENST00000347310.9:c.1714A>G	ENSP00000321345.5:p.Thr572Ala
ENST00000395227.2:c.508A>G	ENSP00000378652.2:p.Thr170Ala
ENST00000425614.3:c.949A>G	ENSP00000387640.2:p.Thr317Ala
ENST00000473881.2:c.*540A>G	ENSP00000486667.1:n.*540A>G
NM_144701.2:c.1714A>G	NP_653302.2:p.Thr572Ala
XM_005270516.2:c.952A>G	XP_005270573.1:p.Thr318Ala
XM_011540789.1:c.1804A>G	XP_011539091.1:p.Thr602Ala
XM_011540790.1:c.1714A>G	XP_011539092.1:p.Thr572Ala
XM_011540791.1:c.1714A>G	XP_011539093.1:p.Thr572Ala
XM_011540790.3:c.1714A>G	XP_011539092.1:p.Thr572Ala
XM_011540791.3:c.1714A>G	XP_011539093.1:p.Thr572Ala
XR_001736993.1:n.1794A>G
NM_144701.3:c.1714A>G MANE Select	NP_653302.2:p.Thr572Ala