Canonical Allele Identifier: CA340729726

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724734T>G (hg19) ; chr1:g.67259051T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259051T>G , CM000663.2:g.67259051T>G	GRCh38
NC_000001.10:g.67724734T>G , CM000663.1:g.67724734T>G	GRCh37
NC_000001.9:g.67497322T>G	NCBI36
NG_011498.1:g.97566T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1652T>G	ENSP00000513138.1:n.1652T>G
ENST00000697150.1:c.1710T>G	ENSP00000513139.1:n.1710T>G
ENST00000697151.1:c.1643T>G	ENSP00000513140.1:n.1643T>G
ENST00000697164.1:c.1723T>G	ENSP00000513153.1:p.Leu575Val
ENST00000697165.1:c.1510T>G	ENSP00000513154.1:p.Leu504Val
ENST00000347310.10:c.1813T>G MANE Select	ENSP00000321345.5:p.Leu605Val
ENST00000637002.1:c.1204T>G	ENSP00000490340.1:p.Leu402Val
ENST00000347310.9:c.1813T>G	ENSP00000321345.5:p.Leu605Val
ENST00000395227.2:c.607T>G	ENSP00000378652.2:p.Leu203Val
ENST00000425614.3:c.1048T>G	ENSP00000387640.2:p.Leu350Val
ENST00000473881.2:c.*639T>G	ENSP00000486667.1:n.*639T>G
NM_144701.2:c.1813T>G	NP_653302.2:p.Leu605Val
XM_005270516.2:c.1051T>G	XP_005270573.1:p.Leu351Val
XM_011540789.1:c.1903T>G	XP_011539091.1:p.Leu635Val
XM_011540790.1:c.1813T>G	XP_011539092.1:p.Leu605Val
XM_011540791.1:c.1813T>G	XP_011539093.1:p.Leu605Val
XM_011540790.3:c.1813T>G	XP_011539092.1:p.Leu605Val
XM_011540791.3:c.1813T>G	XP_011539093.1:p.Leu605Val
XR_001736993.1:n.1893T>G
NM_144701.3:c.1813T>G MANE Select	NP_653302.2:p.Leu605Val