Canonical Allele Identifier: CA340729553

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259004-T-C
• MyVariant Identifiers: chr1:g.67724687T>C (hg19) ; chr1:g.67259004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259004T>C , CM000663.2:g.67259004T>C	GRCh38
NC_000001.10:g.67724687T>C , CM000663.1:g.67724687T>C	GRCh37
NC_000001.9:g.67497275T>C	NCBI36
NG_011498.1:g.97519T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1605T>C	ENSP00000513138.1:n.1605T>C
ENST00000697150.1:c.1663T>C	ENSP00000513139.1:n.1663T>C
ENST00000697151.1:c.1596T>C	ENSP00000513140.1:n.1596T>C
ENST00000697164.1:c.1676T>C	ENSP00000513153.1:p.Leu559Pro
ENST00000697165.1:c.1463T>C	ENSP00000513154.1:p.Leu488Pro
ENST00000347310.10:c.1766T>C MANE Select	ENSP00000321345.5:p.Leu589Pro
ENST00000637002.1:c.1157T>C	ENSP00000490340.1:p.Leu386Pro
ENST00000347310.9:c.1766T>C	ENSP00000321345.5:p.Leu589Pro
ENST00000395227.2:c.560T>C	ENSP00000378652.2:p.Leu187Pro
ENST00000425614.3:c.1001T>C	ENSP00000387640.2:p.Leu334Pro
ENST00000473881.2:c.*592T>C	ENSP00000486667.1:n.*592T>C
NM_144701.2:c.1766T>C	NP_653302.2:p.Leu589Pro
XM_005270516.2:c.1004T>C	XP_005270573.1:p.Leu335Pro
XM_011540789.1:c.1856T>C	XP_011539091.1:p.Leu619Pro
XM_011540790.1:c.1766T>C	XP_011539092.1:p.Leu589Pro
XM_011540791.1:c.1766T>C	XP_011539093.1:p.Leu589Pro
XM_011540790.3:c.1766T>C	XP_011539092.1:p.Leu589Pro
XM_011540791.3:c.1766T>C	XP_011539093.1:p.Leu589Pro
XR_001736993.1:n.1846T>C
NM_144701.3:c.1766T>C MANE Select	NP_653302.2:p.Leu589Pro