Canonical Allele Identifier: CA2338188914
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949243G= , CM000681.2:g.44949243G= GRCh38
NC_000019.9:g.45452500G= , CM000681.1:g.45452500G= GRCh37
NC_000019.8:g.50144340G= NCBI36
NG_008837.1:g.8258G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.300G= (APOC2) MANE Select ENSP00000252490.5:p.Glu100=
ENST00000252490.5:c.300G= (APOC4-APOC2) ENSP00000252490.4:p.Glu100=
ENST00000585685.5:c.*1083G= (APOC4-APOC2) ENSP00000467185.1:n.*1083G=
ENST00000585786.1:c.*379G= (APOC2) ENSP00000465001.1:n.*379G=
ENST00000589057.5:c.531G= (APOC4-APOC2) ENSP00000468139.1:p.Glu177=
ENST00000590360.2:c.300G= (APOC2) ENSP00000466775.1:p.Glu100=
ENST00000591597.5:c.258G= (APOC2) ENSP00000476835.1:p.Glu86=
ENST00000592257.5:c.*94G= (APOC2) ENSP00000477261.1:n.*94G=
NM_000483.4:c.300G= (APOC2) NP_000474.2:p.Glu100=
NR_037932.1:n.1507G= (APOC4-APOC2)
NM_000483.5:c.300G= (APOC2) MANE Select NP_000474.2:p.Glu100=