Canonical Allele Identifier: CA340729683

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724722G>T (hg19) ; chr1:g.67259039G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259039G>T , CM000663.2:g.67259039G>T	GRCh38
NC_000001.10:g.67724722G>T , CM000663.1:g.67724722G>T	GRCh37
NC_000001.9:g.67497310G>T	NCBI36
NG_011498.1:g.97554G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1640G>T	ENSP00000513138.1:n.1640G>T
ENST00000697150.1:c.1698G>T	ENSP00000513139.1:n.1698G>T
ENST00000697151.1:c.1631G>T	ENSP00000513140.1:n.1631G>T
ENST00000697164.1:c.1711G>T	ENSP00000513153.1:p.Val571Leu
ENST00000697165.1:c.1498G>T	ENSP00000513154.1:p.Val500Leu
ENST00000347310.10:c.1801G>T MANE Select	ENSP00000321345.5:p.Val601Leu
ENST00000637002.1:c.1192G>T	ENSP00000490340.1:p.Val398Leu
ENST00000347310.9:c.1801G>T	ENSP00000321345.5:p.Val601Leu
ENST00000395227.2:c.595G>T	ENSP00000378652.2:p.Val199Leu
ENST00000425614.3:c.1036G>T	ENSP00000387640.2:p.Val346Leu
ENST00000473881.2:c.*627G>T	ENSP00000486667.1:n.*627G>T
NM_144701.2:c.1801G>T	NP_653302.2:p.Val601Leu
XM_005270516.2:c.1039G>T	XP_005270573.1:p.Val347Leu
XM_011540789.1:c.1891G>T	XP_011539091.1:p.Val631Leu
XM_011540790.1:c.1801G>T	XP_011539092.1:p.Val601Leu
XM_011540791.1:c.1801G>T	XP_011539093.1:p.Val601Leu
XM_011540790.3:c.1801G>T	XP_011539092.1:p.Val601Leu
XM_011540791.3:c.1801G>T	XP_011539093.1:p.Val601Leu
XR_001736993.1:n.1881G>T
NM_144701.3:c.1801G>T MANE Select	NP_653302.2:p.Val601Leu