Canonical Allele Identifier: CA340729649

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724714T>C (hg19) ; chr1:g.67259031T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259031T>C , CM000663.2:g.67259031T>C	GRCh38
NC_000001.10:g.67724714T>C , CM000663.1:g.67724714T>C	GRCh37
NC_000001.9:g.67497302T>C	NCBI36
NG_011498.1:g.97546T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1632T>C	ENSP00000513138.1:n.1632T>C
ENST00000697150.1:c.1690T>C	ENSP00000513139.1:n.1690T>C
ENST00000697151.1:c.1623T>C	ENSP00000513140.1:n.1623T>C
ENST00000697164.1:c.1703T>C	ENSP00000513153.1:p.Leu568Ser
ENST00000697165.1:c.1490T>C	ENSP00000513154.1:p.Leu497Ser
ENST00000347310.10:c.1793T>C MANE Select	ENSP00000321345.5:p.Leu598Ser
ENST00000637002.1:c.1184T>C	ENSP00000490340.1:p.Leu395Ser
ENST00000347310.9:c.1793T>C	ENSP00000321345.5:p.Leu598Ser
ENST00000395227.2:c.587T>C	ENSP00000378652.2:p.Leu196Ser
ENST00000425614.3:c.1028T>C	ENSP00000387640.2:p.Leu343Ser
ENST00000473881.2:c.*619T>C	ENSP00000486667.1:n.*619T>C
NM_144701.2:c.1793T>C	NP_653302.2:p.Leu598Ser
XM_005270516.2:c.1031T>C	XP_005270573.1:p.Leu344Ser
XM_011540789.1:c.1883T>C	XP_011539091.1:p.Leu628Ser
XM_011540790.1:c.1793T>C	XP_011539092.1:p.Leu598Ser
XM_011540791.1:c.1793T>C	XP_011539093.1:p.Leu598Ser
XM_011540790.3:c.1793T>C	XP_011539092.1:p.Leu598Ser
XM_011540791.3:c.1793T>C	XP_011539093.1:p.Leu598Ser
XR_001736993.1:n.1873T>C
NM_144701.3:c.1793T>C MANE Select	NP_653302.2:p.Leu598Ser