Canonical Allele Identifier: CA340730221

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724810A>G (hg19) ; chr1:g.67259127A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259127A>G , CM000663.2:g.67259127A>G	GRCh38
NC_000001.10:g.67724810A>G , CM000663.1:g.67724810A>G	GRCh37
NC_000001.9:g.67497398A>G	NCBI36
NG_011498.1:g.97642A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697164.1:c.1799A>G	ENSP00000513153.1:p.Ter600Trp
ENST00000697165.1:c.1586A>G	ENSP00000513154.1:p.Ter529Trp
ENST00000347310.10:c.1889A>G MANE Select	ENSP00000321345.5:p.Ter630Trp
ENST00000637002.1:c.1280A>G	ENSP00000490340.1:p.Ter427Trp
ENST00000347310.9:c.1889A>G	ENSP00000321345.5:p.Ter630Trp
ENST00000395227.2:c.683A>G	ENSP00000378652.2:p.Ter228Trp
ENST00000425614.3:c.1124A>G	ENSP00000387640.2:p.Ter375Trp
ENST00000473881.2:c.*715A>G	ENSP00000486667.1:n.*715A>G
NM_144701.2:c.1889A>G	NP_653302.2:p.Ter630Trp
XM_005270516.2:c.1127A>G	XP_005270573.1:p.Ter376Trp
XM_011540789.1:c.1979A>G	XP_011539091.1:p.Ter660Trp
XM_011540790.1:c.1889A>G	XP_011539092.1:p.Ter630Trp
XM_011540791.1:c.1889A>G	XP_011539093.1:p.Ter630Trp
XM_011540790.3:c.1889A>G	XP_011539092.1:p.Ter630Trp
XM_011540791.3:c.1889A>G	XP_011539093.1:p.Ter630Trp
NM_144701.3:c.1889A>G MANE Select	NP_653302.2:p.Ter630Trp