Canonical Allele Identifier: CA340728596

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724426A>C (hg19) ; chr1:g.67258743A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258743A>C , CM000663.2:g.67258743A>C	GRCh38
NC_000001.10:g.67724426A>C , CM000663.1:g.67724426A>C	GRCh37
NC_000001.9:g.67497014A>C	NCBI36
NG_011498.1:g.97258A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1344A>C	ENSP00000513138.1:n.1344A>C
ENST00000697150.1:c.1402A>C	ENSP00000513139.1:n.1402A>C
ENST00000697151.1:c.1335A>C	ENSP00000513140.1:n.1335A>C
ENST00000697164.1:c.1415A>C	ENSP00000513153.1:p.Asn472Thr
ENST00000697165.1:c.1202A>C	ENSP00000513154.1:p.Asn401Thr
ENST00000347310.10:c.1505A>C MANE Select	ENSP00000321345.5:p.Asn502Thr
ENST00000637002.1:c.896A>C	ENSP00000490340.1:p.Asn299Thr
ENST00000347310.9:c.1505A>C	ENSP00000321345.5:p.Asn502Thr
ENST00000395227.2:c.299A>C	ENSP00000378652.2:p.Asn100Thr
ENST00000425614.3:c.740A>C	ENSP00000387640.2:p.Asn247Thr
ENST00000473881.2:c.*331A>C	ENSP00000486667.1:n.*331A>C
NM_144701.2:c.1505A>C	NP_653302.2:p.Asn502Thr
XM_005270516.2:c.743A>C	XP_005270573.1:p.Asn248Thr
XM_011540789.1:c.1595A>C	XP_011539091.1:p.Asn532Thr
XM_011540790.1:c.1505A>C	XP_011539092.1:p.Asn502Thr
XM_011540791.1:c.1505A>C	XP_011539093.1:p.Asn502Thr
XM_011540790.3:c.1505A>C	XP_011539092.1:p.Asn502Thr
XM_011540791.3:c.1505A>C	XP_011539093.1:p.Asn502Thr
XR_001736993.1:n.1585A>C
NM_144701.3:c.1505A>C MANE Select	NP_653302.2:p.Asn502Thr