Canonical Allele Identifier: CA340728713

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258797-A-G
• MyVariant Identifiers: chr1:g.67724480A>G (hg19) ; chr1:g.67258797A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258797A>G , CM000663.2:g.67258797A>G	GRCh38
NC_000001.10:g.67724480A>G , CM000663.1:g.67724480A>G	GRCh37
NC_000001.9:g.67497068A>G	NCBI36
NG_011498.1:g.97312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1398A>G	ENSP00000513138.1:n.1398A>G
ENST00000697150.1:c.1456A>G	ENSP00000513139.1:n.1456A>G
ENST00000697151.1:c.1389A>G	ENSP00000513140.1:n.1389A>G
ENST00000697164.1:c.1469A>G	ENSP00000513153.1:p.Asn490Ser
ENST00000697165.1:c.1256A>G	ENSP00000513154.1:p.Asn419Ser
ENST00000347310.10:c.1559A>G MANE Select	ENSP00000321345.5:p.Asn520Ser
ENST00000637002.1:c.950A>G	ENSP00000490340.1:p.Asn317Ser
ENST00000347310.9:c.1559A>G	ENSP00000321345.5:p.Asn520Ser
ENST00000395227.2:c.353A>G	ENSP00000378652.2:p.Asn118Ser
ENST00000425614.3:c.794A>G	ENSP00000387640.2:p.Asn265Ser
ENST00000473881.2:c.*385A>G	ENSP00000486667.1:n.*385A>G
NM_144701.2:c.1559A>G	NP_653302.2:p.Asn520Ser
XM_005270516.2:c.797A>G	XP_005270573.1:p.Asn266Ser
XM_011540789.1:c.1649A>G	XP_011539091.1:p.Asn550Ser
XM_011540790.1:c.1559A>G	XP_011539092.1:p.Asn520Ser
XM_011540791.1:c.1559A>G	XP_011539093.1:p.Asn520Ser
XM_011540790.3:c.1559A>G	XP_011539092.1:p.Asn520Ser
XM_011540791.3:c.1559A>G	XP_011539093.1:p.Asn520Ser
XR_001736993.1:n.1639A>G
NM_144701.3:c.1559A>G MANE Select	NP_653302.2:p.Asn520Ser