Canonical Allele Identifier: CA340729787

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724747A>G (hg19) ; chr1:g.67259064A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259064A>G , CM000663.2:g.67259064A>G	GRCh38
NC_000001.10:g.67724747A>G , CM000663.1:g.67724747A>G	GRCh37
NC_000001.9:g.67497335A>G	NCBI36
NG_011498.1:g.97579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1665A>G	ENSP00000513138.1:n.1665A>G
ENST00000697150.1:c.1723A>G	ENSP00000513139.1:n.1723A>G
ENST00000697151.1:c.1656A>G	ENSP00000513140.1:n.1656A>G
ENST00000697164.1:c.1736A>G	ENSP00000513153.1:p.Asn579Ser
ENST00000697165.1:c.1523A>G	ENSP00000513154.1:p.Asn508Ser
ENST00000347310.10:c.1826A>G MANE Select	ENSP00000321345.5:p.Asn609Ser
ENST00000637002.1:c.1217A>G	ENSP00000490340.1:p.Asn406Ser
ENST00000347310.9:c.1826A>G	ENSP00000321345.5:p.Asn609Ser
ENST00000395227.2:c.620A>G	ENSP00000378652.2:p.Asn207Ser
ENST00000425614.3:c.1061A>G	ENSP00000387640.2:p.Asn354Ser
ENST00000473881.2:c.*652A>G	ENSP00000486667.1:n.*652A>G
NM_144701.2:c.1826A>G	NP_653302.2:p.Asn609Ser
XM_005270516.2:c.1064A>G	XP_005270573.1:p.Asn355Ser
XM_011540789.1:c.1916A>G	XP_011539091.1:p.Asn639Ser
XM_011540790.1:c.1826A>G	XP_011539092.1:p.Asn609Ser
XM_011540791.1:c.1826A>G	XP_011539093.1:p.Asn609Ser
XM_011540790.3:c.1826A>G	XP_011539092.1:p.Asn609Ser
XM_011540791.3:c.1826A>G	XP_011539093.1:p.Asn609Ser
XR_001736993.1:n.1906A>G
NM_144701.3:c.1826A>G MANE Select	NP_653302.2:p.Asn609Ser