Canonical Allele Identifier: CA340725886

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67705934T>G (hg19) ; chr1:g.67240251T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240251T>G , CM000663.2:g.67240251T>G	GRCh38
NC_000001.10:g.67705934T>G , CM000663.1:g.67705934T>G	GRCh37
NC_000001.9:g.67478522T>G	NCBI36
NG_011498.1:g.78766T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.994T>G	ENSP00000513137.1:n.994T>G
ENST00000697149.1:c.957T>G	ENSP00000513138.1:n.957T>G
ENST00000697150.1:c.1045+3449T>G	ENSP00000513139.1:n.1045+3449T>G
ENST00000697151.1:c.1045+3449T>G	ENSP00000513140.1:n.1045+3449T>G
ENST00000697152.1:c.799-15586T>G	ENSP00000513141.1:n.799-15586T>G
ENST00000697153.1:c.795-15586T>G	ENSP00000513142.1:n.795-15586T>G
ENST00000697154.1:c.956-18227T>G	ENSP00000513143.1:n.956-18227T>G
ENST00000697155.1:c.649-18227T>G	ENSP00000513144.1:n.649-18227T>G
ENST00000697156.1:c.1118T>G	ENSP00000513145.1:p.Ile373Ser
ENST00000697157.1:c.972T>G	ENSP00000513146.1:n.972T>G
ENST00000697158.1:c.961T>G	ENSP00000513147.1:n.961T>G
ENST00000697159.1:c.811T>G	ENSP00000513148.1:n.811T>G
ENST00000697160.1:c.956-15586T>G	ENSP00000513149.1:n.956-15586T>G
ENST00000697161.1:c.654T>G	ENSP00000513150.1:n.654T>G
ENST00000697162.1:c.1047T>G	ENSP00000513151.1:n.1047T>G
ENST00000697163.1:c.1118T>G	ENSP00000513152.1:p.Ile373Ser
ENST00000697164.1:c.1028T>G	ENSP00000513153.1:p.Ile343Ser
ENST00000697165.1:c.815T>G	ENSP00000513154.1:p.Ile272Ser
ENST00000697223.1:c.867T>G	ENSP00000513190.1:n.867T>G
ENST00000697224.1:c.884+3449T>G	ENSP00000513191.1:n.884+3449T>G
ENST00000697225.1:c.721T>G	ENSP00000513192.1:n.721T>G
ENST00000697226.1:c.738+3449T>G	ENSP00000513193.1:n.738+3449T>G
ENST00000697227.1:c.954T>G	ENSP00000513194.1:n.954T>G
ENST00000697228.1:c.810T>G	ENSP00000513195.1:n.810T>G
ENST00000697229.1:c.885-15586T>G	ENSP00000513196.1:n.885-15586T>G
ENST00000697230.1:c.1028T>G	ENSP00000513197.1:p.Ile343Ser
ENST00000697231.1:c.1023T>G	ENSP00000513198.1:n.1023T>G
ENST00000697232.1:c.1047T>G	ENSP00000513199.1:n.1047T>G
ENST00000347310.10:c.1118T>G MANE Select	ENSP00000321345.5:p.Ile373Ser
ENST00000637002.1:c.509T>G	ENSP00000490340.1:p.Ile170Ser
ENST00000347310.9:c.1118T>G	ENSP00000321345.5:p.Ile373Ser
ENST00000395227.2:c.-58-15586T>G	ENSP00000378652.2:n.-58-15586T>G
ENST00000425614.3:c.353T>G	ENSP00000387640.2:p.Ile118Ser
ENST00000473881.2:c.191-15586T>G	ENSP00000486667.1:n.191-15586T>G
NM_144701.2:c.1118T>G	NP_653302.2:p.Ile373Ser
XM_005270516.2:c.356T>G	XP_005270573.1:p.Ile119Ser
XM_011540789.1:c.1208T>G	XP_011539091.1:p.Ile403Ser
XM_011540790.1:c.1118T>G	XP_011539092.1:p.Ile373Ser
XM_011540791.1:c.1118T>G	XP_011539093.1:p.Ile373Ser
XM_011540790.3:c.1118T>G	XP_011539092.1:p.Ile373Ser
XM_011540791.3:c.1118T>G	XP_011539093.1:p.Ile373Ser
XR_001736993.1:n.1228+3449T>G
NM_144701.3:c.1118T>G MANE Select	NP_653302.2:p.Ile373Ser