Canonical Allele Identifier: CA340729778

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259063-A-T
• MyVariant Identifiers: chr1:g.67724746A>T (hg19) ; chr1:g.67259063A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259063A>T , CM000663.2:g.67259063A>T	GRCh38
NC_000001.10:g.67724746A>T , CM000663.1:g.67724746A>T	GRCh37
NC_000001.9:g.67497334A>T	NCBI36
NG_011498.1:g.97578A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1664A>T	ENSP00000513138.1:n.1664A>T
ENST00000697150.1:c.1722A>T	ENSP00000513139.1:n.1722A>T
ENST00000697151.1:c.1655A>T	ENSP00000513140.1:n.1655A>T
ENST00000697164.1:c.1735A>T	ENSP00000513153.1:p.Asn579Tyr
ENST00000697165.1:c.1522A>T	ENSP00000513154.1:p.Asn508Tyr
ENST00000347310.10:c.1825A>T MANE Select	ENSP00000321345.5:p.Asn609Tyr
ENST00000637002.1:c.1216A>T	ENSP00000490340.1:p.Asn406Tyr
ENST00000347310.9:c.1825A>T	ENSP00000321345.5:p.Asn609Tyr
ENST00000395227.2:c.619A>T	ENSP00000378652.2:p.Asn207Tyr
ENST00000425614.3:c.1060A>T	ENSP00000387640.2:p.Asn354Tyr
ENST00000473881.2:c.*651A>T	ENSP00000486667.1:n.*651A>T
NM_144701.2:c.1825A>T	NP_653302.2:p.Asn609Tyr
XM_005270516.2:c.1063A>T	XP_005270573.1:p.Asn355Tyr
XM_011540789.1:c.1915A>T	XP_011539091.1:p.Asn639Tyr
XM_011540790.1:c.1825A>T	XP_011539092.1:p.Asn609Tyr
XM_011540791.1:c.1825A>T	XP_011539093.1:p.Asn609Tyr
XM_011540790.3:c.1825A>T	XP_011539092.1:p.Asn609Tyr
XM_011540791.3:c.1825A>T	XP_011539093.1:p.Asn609Tyr
XR_001736993.1:n.1905A>T
NM_144701.3:c.1825A>T MANE Select	NP_653302.2:p.Asn609Tyr