Canonical Allele Identifier: CA2338188903
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949205A= , CM000681.2:g.44949205A= GRCh38
NC_000019.9:g.45452462A= , CM000681.1:g.45452462A= GRCh37
NC_000019.8:g.50144302A= NCBI36
NG_008837.1:g.8220A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.262A= (APOC2) MANE Select ENSP00000252490.5:p.Ile88=
ENST00000252490.5:c.262A= (APOC4-APOC2) ENSP00000252490.4:p.Ile88=
ENST00000585685.5:c.*1045A= (APOC4-APOC2) ENSP00000467185.1:n.*1045A=
ENST00000585786.1:c.*341A= (APOC2) ENSP00000465001.1:n.*341A=
ENST00000589057.5:c.493A= (APOC4-APOC2) ENSP00000468139.1:p.Ile165=
ENST00000590360.2:c.262A= (APOC2) ENSP00000466775.1:p.Ile88=
ENST00000591597.5:c.220A= (APOC2) ENSP00000476835.1:p.Ile74=
ENST00000592257.5:c.*56A= (APOC2) ENSP00000477261.1:n.*56A=
NM_000483.4:c.262A= (APOC2) NP_000474.2:p.Ile88=
NR_037932.1:n.1469A= (APOC4-APOC2)
NM_000483.5:c.262A= (APOC2) MANE Select NP_000474.2:p.Ile88=