Canonical Allele Identifier: CA3081745526
Community Standard Title: NM_144701.3(IL23R):c.*199A=
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259327A= , CM000663.2:g.67259327A= GRCh38
NC_000001.10:g.67725010A= , CM000663.1:g.67725010A= GRCh37
NC_000001.9:g.67497598A= NCBI36
NG_011498.1:g.97842A=

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.*199A= MANE Select NP_653302.2:n.*199A=
ENST00000347310.10:c.*199A= MANE Select ENSP00000321345.5:n.*199A=
NM_144701.2:c.*199A= NP_653302.2:n.*199A=
ENST00000347310.9:c.*199A= ENSP00000321345.5:n.*199A=
ENST00000395227.2:c.*199A= ENSP00000378652.2:n.*199A=
ENST00000473881.2:c.*915A= ENSP00000486667.1:n.*915A=
XM_005270516.2:c.*199A= XP_005270573.1:n.*199A=
XM_011540789.1:c.*199A= XP_011539091.1:n.*199A=
XM_011540790.1:c.*199A= XP_011539092.1:n.*199A=
XM_011540790.3:c.*199A= XP_011539092.1:n.*199A=
XM_011540791.1:c.*199A= XP_011539093.1:n.*199A=
XM_011540791.3:c.*199A= XP_011539093.1:n.*199A=