Canonical Allele Identifier: CA340729028

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724567T>C (hg19) ; chr1:g.67258884T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258884T>C , CM000663.2:g.67258884T>C	GRCh38
NC_000001.10:g.67724567T>C , CM000663.1:g.67724567T>C	GRCh37
NC_000001.9:g.67497155T>C	NCBI36
NG_011498.1:g.97399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1485T>C	ENSP00000513138.1:n.1485T>C
ENST00000697150.1:c.1543T>C	ENSP00000513139.1:n.1543T>C
ENST00000697151.1:c.1476T>C	ENSP00000513140.1:n.1476T>C
ENST00000697164.1:c.1556T>C	ENSP00000513153.1:p.Leu519Ser
ENST00000697165.1:c.1343T>C	ENSP00000513154.1:p.Leu448Ser
ENST00000347310.10:c.1646T>C MANE Select	ENSP00000321345.5:p.Leu549Ser
ENST00000637002.1:c.1037T>C	ENSP00000490340.1:p.Leu346Ser
ENST00000347310.9:c.1646T>C	ENSP00000321345.5:p.Leu549Ser
ENST00000395227.2:c.440T>C	ENSP00000378652.2:p.Leu147Ser
ENST00000425614.3:c.881T>C	ENSP00000387640.2:p.Leu294Ser
ENST00000473881.2:c.*472T>C	ENSP00000486667.1:n.*472T>C
NM_144701.2:c.1646T>C	NP_653302.2:p.Leu549Ser
XM_005270516.2:c.884T>C	XP_005270573.1:p.Leu295Ser
XM_011540789.1:c.1736T>C	XP_011539091.1:p.Leu579Ser
XM_011540790.1:c.1646T>C	XP_011539092.1:p.Leu549Ser
XM_011540791.1:c.1646T>C	XP_011539093.1:p.Leu549Ser
XM_011540790.3:c.1646T>C	XP_011539092.1:p.Leu549Ser
XM_011540791.3:c.1646T>C	XP_011539093.1:p.Leu549Ser
XR_001736993.1:n.1726T>C
NM_144701.3:c.1646T>C MANE Select	NP_653302.2:p.Leu549Ser