Canonical Allele Identifier: CA340729903

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724767A>T (hg19) ; chr1:g.67259084A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259084A>T , CM000663.2:g.67259084A>T	GRCh38
NC_000001.10:g.67724767A>T , CM000663.1:g.67724767A>T	GRCh37
NC_000001.9:g.67497355A>T	NCBI36
NG_011498.1:g.97599A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1685A>T	ENSP00000513138.1:n.1685A>T
ENST00000697150.1:c.1743A>T	ENSP00000513139.1:n.1743A>T
ENST00000697151.1:c.1676A>T	ENSP00000513140.1:n.1676A>T
ENST00000697164.1:c.1756A>T	ENSP00000513153.1:p.Ile586Phe
ENST00000697165.1:c.1543A>T	ENSP00000513154.1:p.Ile515Phe
ENST00000347310.10:c.1846A>T MANE Select	ENSP00000321345.5:p.Ile616Phe
ENST00000637002.1:c.1237A>T	ENSP00000490340.1:p.Ile413Phe
ENST00000347310.9:c.1846A>T	ENSP00000321345.5:p.Ile616Phe
ENST00000395227.2:c.640A>T	ENSP00000378652.2:p.Ile214Phe
ENST00000425614.3:c.1081A>T	ENSP00000387640.2:p.Ile361Phe
ENST00000473881.2:c.*672A>T	ENSP00000486667.1:n.*672A>T
NM_144701.2:c.1846A>T	NP_653302.2:p.Ile616Phe
XM_005270516.2:c.1084A>T	XP_005270573.1:p.Ile362Phe
XM_011540789.1:c.1936A>T	XP_011539091.1:p.Ile646Phe
XM_011540790.1:c.1846A>T	XP_011539092.1:p.Ile616Phe
XM_011540791.1:c.1846A>T	XP_011539093.1:p.Ile616Phe
XM_011540790.3:c.1846A>T	XP_011539092.1:p.Ile616Phe
XM_011540791.3:c.1846A>T	XP_011539093.1:p.Ile616Phe
XR_001736993.1:n.1926A>T
NM_144701.3:c.1846A>T MANE Select	NP_653302.2:p.Ile616Phe