Canonical Allele Identifier: CA340729422

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724651A>T (hg19) ; chr1:g.67258968A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258968A>T , CM000663.2:g.67258968A>T	GRCh38
NC_000001.10:g.67724651A>T , CM000663.1:g.67724651A>T	GRCh37
NC_000001.9:g.67497239A>T	NCBI36
NG_011498.1:g.97483A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1569A>T	ENSP00000513138.1:n.1569A>T
ENST00000697150.1:c.1627A>T	ENSP00000513139.1:n.1627A>T
ENST00000697151.1:c.1560A>T	ENSP00000513140.1:n.1560A>T
ENST00000697164.1:c.1640A>T	ENSP00000513153.1:p.Asn547Ile
ENST00000697165.1:c.1427A>T	ENSP00000513154.1:p.Asn476Ile
ENST00000347310.10:c.1730A>T MANE Select	ENSP00000321345.5:p.Asn577Ile
ENST00000637002.1:c.1121A>T	ENSP00000490340.1:p.Asn374Ile
ENST00000347310.9:c.1730A>T	ENSP00000321345.5:p.Asn577Ile
ENST00000395227.2:c.524A>T	ENSP00000378652.2:p.Asn175Ile
ENST00000425614.3:c.965A>T	ENSP00000387640.2:p.Asn322Ile
ENST00000473881.2:c.*556A>T	ENSP00000486667.1:n.*556A>T
NM_144701.2:c.1730A>T	NP_653302.2:p.Asn577Ile
XM_005270516.2:c.968A>T	XP_005270573.1:p.Asn323Ile
XM_011540789.1:c.1820A>T	XP_011539091.1:p.Asn607Ile
XM_011540790.1:c.1730A>T	XP_011539092.1:p.Asn577Ile
XM_011540791.1:c.1730A>T	XP_011539093.1:p.Asn577Ile
XM_011540790.3:c.1730A>T	XP_011539092.1:p.Asn577Ile
XM_011540791.3:c.1730A>T	XP_011539093.1:p.Asn577Ile
XR_001736993.1:n.1810A>T
NM_144701.3:c.1730A>T MANE Select	NP_653302.2:p.Asn577Ile