Canonical Allele Identifier: CA340729752
Community Standard Title: NM_144701.3(IL23R):c.1819T>G (p.Ser607Ala)
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259057T>G , CM000663.2:g.67259057T>G GRCh38
NC_000001.10:g.67724740T>G , CM000663.1:g.67724740T>G GRCh37
NC_000001.9:g.67497328T>G NCBI36
NG_011498.1:g.97572T>G

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.1819T>G MANE Select NP_653302.2:p.Ser607Ala
ENST00000347310.10:c.1819T>G MANE Select ENSP00000321345.5:p.Ser607Ala
NM_144701.2:c.1819T>G NP_653302.2:p.Ser607Ala
ENST00000347310.9:c.1819T>G ENSP00000321345.5:p.Ser607Ala
ENST00000395227.2:c.613T>G ENSP00000378652.2:p.Ser205Ala
ENST00000425614.3:c.1054T>G ENSP00000387640.2:p.Ser352Ala
ENST00000473881.2:c.*645T>G ENSP00000486667.1:n.*645T>G
ENST00000637002.1:c.1210T>G ENSP00000490340.1:p.Ser404Ala
ENST00000697149.1:c.1658T>G ENSP00000513138.1:n.1658T>G
ENST00000697150.1:c.1716T>G ENSP00000513139.1:n.1716T>G
ENST00000697151.1:c.1649T>G ENSP00000513140.1:n.1649T>G
ENST00000697164.1:c.1729T>G ENSP00000513153.1:p.Ser577Ala
ENST00000697165.1:c.1516T>G ENSP00000513154.1:p.Ser506Ala
XM_005270516.2:c.1057T>G XP_005270573.1:p.Ser353Ala
XM_011540789.1:c.1909T>G XP_011539091.1:p.Ser637Ala
XM_011540790.1:c.1819T>G XP_011539092.1:p.Ser607Ala
XM_011540790.3:c.1819T>G XP_011539092.1:p.Ser607Ala
XM_011540791.1:c.1819T>G XP_011539093.1:p.Ser607Ala
XM_011540791.3:c.1819T>G XP_011539093.1:p.Ser607Ala
XR_001736993.1:n.1899T>G