Canonical Allele Identifier: CA340729426

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724653G>T (hg19) ; chr1:g.67258970G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258970G>T , CM000663.2:g.67258970G>T	GRCh38
NC_000001.10:g.67724653G>T , CM000663.1:g.67724653G>T	GRCh37
NC_000001.9:g.67497241G>T	NCBI36
NG_011498.1:g.97485G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1571G>T	ENSP00000513138.1:n.1571G>T
ENST00000697150.1:c.1629G>T	ENSP00000513139.1:n.1629G>T
ENST00000697151.1:c.1562G>T	ENSP00000513140.1:n.1562G>T
ENST00000697164.1:c.1642G>T	ENSP00000513153.1:p.Asp548Tyr
ENST00000697165.1:c.1429G>T	ENSP00000513154.1:p.Asp477Tyr
ENST00000347310.10:c.1732G>T MANE Select	ENSP00000321345.5:p.Asp578Tyr
ENST00000637002.1:c.1123G>T	ENSP00000490340.1:p.Asp375Tyr
ENST00000347310.9:c.1732G>T	ENSP00000321345.5:p.Asp578Tyr
ENST00000395227.2:c.526G>T	ENSP00000378652.2:p.Asp176Tyr
ENST00000425614.3:c.967G>T	ENSP00000387640.2:p.Asp323Tyr
ENST00000473881.2:c.*558G>T	ENSP00000486667.1:n.*558G>T
NM_144701.2:c.1732G>T	NP_653302.2:p.Asp578Tyr
XM_005270516.2:c.970G>T	XP_005270573.1:p.Asp324Tyr
XM_011540789.1:c.1822G>T	XP_011539091.1:p.Asp608Tyr
XM_011540790.1:c.1732G>T	XP_011539092.1:p.Asp578Tyr
XM_011540791.1:c.1732G>T	XP_011539093.1:p.Asp578Tyr
XM_011540790.3:c.1732G>T	XP_011539092.1:p.Asp578Tyr
XM_011540791.3:c.1732G>T	XP_011539093.1:p.Asp578Tyr
XR_001736993.1:n.1812G>T
NM_144701.3:c.1732G>T MANE Select	NP_653302.2:p.Asp578Tyr