Canonical Allele Identifier: CA340729807

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259067-C-T
• MyVariant Identifiers: chr1:g.67724750C>T (hg19) ; chr1:g.67259067C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259067C>T , CM000663.2:g.67259067C>T	GRCh38
NC_000001.10:g.67724750C>T , CM000663.1:g.67724750C>T	GRCh37
NC_000001.9:g.67497338C>T	NCBI36
NG_011498.1:g.97582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1668C>T	ENSP00000513138.1:n.1668C>T
ENST00000697150.1:c.1726C>T	ENSP00000513139.1:n.1726C>T
ENST00000697151.1:c.1659C>T	ENSP00000513140.1:n.1659C>T
ENST00000697164.1:c.1739C>T	ENSP00000513153.1:p.Thr580Ile
ENST00000697165.1:c.1526C>T	ENSP00000513154.1:p.Thr509Ile
ENST00000347310.10:c.1829C>T MANE Select	ENSP00000321345.5:p.Thr610Ile
ENST00000637002.1:c.1220C>T	ENSP00000490340.1:p.Thr407Ile
ENST00000347310.9:c.1829C>T	ENSP00000321345.5:p.Thr610Ile
ENST00000395227.2:c.623C>T	ENSP00000378652.2:p.Thr208Ile
ENST00000425614.3:c.1064C>T	ENSP00000387640.2:p.Thr355Ile
ENST00000473881.2:c.*655C>T	ENSP00000486667.1:n.*655C>T
NM_144701.2:c.1829C>T	NP_653302.2:p.Thr610Ile
XM_005270516.2:c.1067C>T	XP_005270573.1:p.Thr356Ile
XM_011540789.1:c.1919C>T	XP_011539091.1:p.Thr640Ile
XM_011540790.1:c.1829C>T	XP_011539092.1:p.Thr610Ile
XM_011540791.1:c.1829C>T	XP_011539093.1:p.Thr610Ile
XM_011540790.3:c.1829C>T	XP_011539092.1:p.Thr610Ile
XM_011540791.3:c.1829C>T	XP_011539093.1:p.Thr610Ile
XR_001736993.1:n.1909C>T
NM_144701.3:c.1829C>T MANE Select	NP_653302.2:p.Thr610Ile