Canonical Allele Identifier: CA8586755
Gene: AOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42852148C>T , CM000679.2:g.42852148C>T GRCh38
NC_000017.10:g.41004165C>T , CM000679.1:g.41004165C>T GRCh37
NC_000017.9:g.38257691C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003734.4:c.805C>T MANE Select NP_003725.1:p.Arg269Cys
ENST00000308423.7:c.805C>T MANE Select ENSP00000312326.1:p.Arg269Cys
NM_001277731.1:c.805C>T NP_001264660.1:p.Arg269Cys
NM_001277731.2:c.805C>T NP_001264660.1:p.Arg269Cys
NM_003734.3:c.805C>T NP_003725.1:p.Arg269Cys
NR_102422.1:n.965C>T
NR_102422.2:n.950C>T
ENST00000308423.6:c.805C>T ENSP00000312326.1:p.Arg269Cys
ENST00000613571.1:c.805C>T ENSP00000484312.1:p.Arg269Cys
XM_011525419.1:c.805C>T XP_011523721.1:p.Arg269Cys
XM_011525419.2:c.805C>T XP_011523721.1:p.Arg269Cys
XM_011525420.1:c.805C>T XP_011523722.1:p.Arg269Cys
XM_011525420.3:c.805C>T XP_011523722.1:p.Arg269Cys
XR_001752673.2:n.967C>T
XR_934584.1:n.1026C>T
XR_934584.2:n.967C>T