Canonical Allele Identifier: CA340729365

Gene: IL23R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1553A>T	ENSP00000513138.1:n.1553A>T
ENST00000697150.1:c.1611A>T	ENSP00000513139.1:n.1611A>T
ENST00000697151.1:c.1544A>T	ENSP00000513140.1:n.1544A>T
ENST00000697164.1:c.1624A>T	ENSP00000513153.1:p.Thr542Ser
ENST00000697165.1:c.1411A>T	ENSP00000513154.1:p.Thr471Ser
ENST00000347310.10:c.1714A>T MANE Select	ENSP00000321345.5:p.Thr572Ser
ENST00000637002.1:c.1105A>T	ENSP00000490340.1:p.Thr369Ser
ENST00000347310.9:c.1714A>T	ENSP00000321345.5:p.Thr572Ser
ENST00000395227.2:c.508A>T	ENSP00000378652.2:p.Thr170Ser
ENST00000425614.3:c.949A>T	ENSP00000387640.2:p.Thr317Ser
ENST00000473881.2:c.*540A>T	ENSP00000486667.1:n.*540A>T
NM_144701.2:c.1714A>T	NP_653302.2:p.Thr572Ser
XM_005270516.2:c.952A>T	XP_005270573.1:p.Thr318Ser
XM_011540789.1:c.1804A>T	XP_011539091.1:p.Thr602Ser
XM_011540790.1:c.1714A>T	XP_011539092.1:p.Thr572Ser
XM_011540791.1:c.1714A>T	XP_011539093.1:p.Thr572Ser
XM_011540790.3:c.1714A>T	XP_011539092.1:p.Thr572Ser
XM_011540791.3:c.1714A>T	XP_011539093.1:p.Thr572Ser
XR_001736993.1:n.1794A>T
NM_144701.3:c.1714A>T MANE Select	NP_653302.2:p.Thr572Ser