Canonical Allele Identifier: CA340728695

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724470G>T (hg19) ; chr1:g.67258787G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258787G>T , CM000663.2:g.67258787G>T	GRCh38
NC_000001.10:g.67724470G>T , CM000663.1:g.67724470G>T	GRCh37
NC_000001.9:g.67497058G>T	NCBI36
NG_011498.1:g.97302G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1388G>T	ENSP00000513138.1:n.1388G>T
ENST00000697150.1:c.1446G>T	ENSP00000513139.1:n.1446G>T
ENST00000697151.1:c.1379G>T	ENSP00000513140.1:n.1379G>T
ENST00000697164.1:c.1459G>T	ENSP00000513153.1:p.Asp487Tyr
ENST00000697165.1:c.1246G>T	ENSP00000513154.1:p.Asp416Tyr
ENST00000347310.10:c.1549G>T MANE Select	ENSP00000321345.5:p.Asp517Tyr
ENST00000637002.1:c.940G>T	ENSP00000490340.1:p.Asp314Tyr
ENST00000347310.9:c.1549G>T	ENSP00000321345.5:p.Asp517Tyr
ENST00000395227.2:c.343G>T	ENSP00000378652.2:p.Asp115Tyr
ENST00000425614.3:c.784G>T	ENSP00000387640.2:p.Asp262Tyr
ENST00000473881.2:c.*375G>T	ENSP00000486667.1:n.*375G>T
NM_144701.2:c.1549G>T	NP_653302.2:p.Asp517Tyr
XM_005270516.2:c.787G>T	XP_005270573.1:p.Asp263Tyr
XM_011540789.1:c.1639G>T	XP_011539091.1:p.Asp547Tyr
XM_011540790.1:c.1549G>T	XP_011539092.1:p.Asp517Tyr
XM_011540791.1:c.1549G>T	XP_011539093.1:p.Asp517Tyr
XM_011540790.3:c.1549G>T	XP_011539092.1:p.Asp517Tyr
XM_011540791.3:c.1549G>T	XP_011539093.1:p.Asp517Tyr
XR_001736993.1:n.1629G>T
NM_144701.3:c.1549G>T MANE Select	NP_653302.2:p.Asp517Tyr