Canonical Allele Identifier: CA340729387

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724640G>C (hg19) ; chr1:g.67258957G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258957G>C , CM000663.2:g.67258957G>C	GRCh38
NC_000001.10:g.67724640G>C , CM000663.1:g.67724640G>C	GRCh37
NC_000001.9:g.67497228G>C	NCBI36
NG_011498.1:g.97472G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1558G>C	ENSP00000513138.1:n.1558G>C
ENST00000697150.1:c.1616G>C	ENSP00000513139.1:n.1616G>C
ENST00000697151.1:c.1549G>C	ENSP00000513140.1:n.1549G>C
ENST00000697164.1:c.1629G>C	ENSP00000513153.1:p.Met543Ile
ENST00000697165.1:c.1416G>C	ENSP00000513154.1:p.Met472Ile
ENST00000347310.10:c.1719G>C MANE Select	ENSP00000321345.5:p.Met573Ile
ENST00000637002.1:c.1110G>C	ENSP00000490340.1:p.Met370Ile
ENST00000347310.9:c.1719G>C	ENSP00000321345.5:p.Met573Ile
ENST00000395227.2:c.513G>C	ENSP00000378652.2:p.Met171Ile
ENST00000425614.3:c.954G>C	ENSP00000387640.2:p.Met318Ile
ENST00000473881.2:c.*545G>C	ENSP00000486667.1:n.*545G>C
NM_144701.2:c.1719G>C	NP_653302.2:p.Met573Ile
XM_005270516.2:c.957G>C	XP_005270573.1:p.Met319Ile
XM_011540789.1:c.1809G>C	XP_011539091.1:p.Met603Ile
XM_011540790.1:c.1719G>C	XP_011539092.1:p.Met573Ile
XM_011540791.1:c.1719G>C	XP_011539093.1:p.Met573Ile
XM_011540790.3:c.1719G>C	XP_011539092.1:p.Met573Ile
XM_011540791.3:c.1719G>C	XP_011539093.1:p.Met573Ile
XR_001736993.1:n.1799G>C
NM_144701.3:c.1719G>C MANE Select	NP_653302.2:p.Met573Ile