Canonical Allele Identifier: CA418438835

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724799C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259116C>G , CM000663.2:g.67259116C>G	GRCh38
NC_000001.10:g.67724799C>G , CM000663.1:g.67724799C>G	GRCh37
NC_000001.9:g.67497387C>G	NCBI36
NG_011498.1:g.97631C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1717C>G	ENSP00000513138.1:n.1717C>G
ENST00000697150.1:c.1775C>G	ENSP00000513139.1:n.1775C>G
ENST00000697151.1:c.1708C>G	ENSP00000513140.1:n.1708C>G
ENST00000697164.1:c.1788C>G	ENSP00000513153.1:p.Leu596=
ENST00000697165.1:c.1575C>G	ENSP00000513154.1:p.Leu525=
ENST00000347310.10:c.1878C>G MANE Select	ENSP00000321345.5:p.Leu626=
ENST00000637002.1:c.1269C>G	ENSP00000490340.1:p.Leu423=
ENST00000347310.9:c.1878C>G	ENSP00000321345.5:p.Leu626=
ENST00000395227.2:c.672C>G	ENSP00000378652.2:p.Leu224=
ENST00000425614.3:c.1113C>G	ENSP00000387640.2:p.Leu371=
ENST00000473881.2:c.*704C>G	ENSP00000486667.1:n.*704C>G
NM_144701.2:c.1878C>G	NP_653302.2:p.Leu626=
XM_005270516.2:c.1116C>G	XP_005270573.1:p.Leu372=
XM_011540789.1:c.1968C>G	XP_011539091.1:p.Leu656=
XM_011540790.1:c.1878C>G	XP_011539092.1:p.Leu626=
XM_011540791.1:c.1878C>G	XP_011539093.1:p.Leu626=
XM_011540790.3:c.1878C>G	XP_011539092.1:p.Leu626=
XM_011540791.3:c.1878C>G	XP_011539093.1:p.Leu626=
XR_001736993.1:n.1958C>G
NM_144701.3:c.1878C>G MANE Select	NP_653302.2:p.Leu626=