Canonical Allele Identifier: CA418438712

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724481T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258798T>C , CM000663.2:g.67258798T>C	GRCh38
NC_000001.10:g.67724481T>C , CM000663.1:g.67724481T>C	GRCh37
NC_000001.9:g.67497069T>C	NCBI36
NG_011498.1:g.97313T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1399T>C	ENSP00000513138.1:n.1399T>C
ENST00000697150.1:c.1457T>C	ENSP00000513139.1:n.1457T>C
ENST00000697151.1:c.1390T>C	ENSP00000513140.1:n.1390T>C
ENST00000697164.1:c.1470T>C	ENSP00000513153.1:p.Asn490=
ENST00000697165.1:c.1257T>C	ENSP00000513154.1:p.Asn419=
ENST00000347310.10:c.1560T>C MANE Select	ENSP00000321345.5:p.Asn520=
ENST00000637002.1:c.951T>C	ENSP00000490340.1:p.Asn317=
ENST00000347310.9:c.1560T>C	ENSP00000321345.5:p.Asn520=
ENST00000395227.2:c.354T>C	ENSP00000378652.2:p.Asn118=
ENST00000425614.3:c.795T>C	ENSP00000387640.2:p.Asn265=
ENST00000473881.2:c.*386T>C	ENSP00000486667.1:n.*386T>C
NM_144701.2:c.1560T>C	NP_653302.2:p.Asn520=
XM_005270516.2:c.798T>C	XP_005270573.1:p.Asn266=
XM_011540789.1:c.1650T>C	XP_011539091.1:p.Asn550=
XM_011540790.1:c.1560T>C	XP_011539092.1:p.Asn520=
XM_011540791.1:c.1560T>C	XP_011539093.1:p.Asn520=
XM_011540790.3:c.1560T>C	XP_011539092.1:p.Asn520=
XM_011540791.3:c.1560T>C	XP_011539093.1:p.Asn520=
XR_001736993.1:n.1640T>C
NM_144701.3:c.1560T>C MANE Select	NP_653302.2:p.Asn520=