Canonical Allele Identifier: CA2338188661
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948502T= , CM000681.2:g.44948502T= GRCh38
NC_000019.9:g.45451759T= , CM000681.1:g.45451759T= GRCh37
NC_000019.8:g.50143599T= NCBI36
NG_008837.1:g.7517T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.24T= (APOC2) MANE Select ENSP00000252490.5:p.Ala8=
ENST00000252490.5:c.24T= (APOC4-APOC2) ENSP00000252490.4:p.Ala8=
ENST00000585685.5:c.*807T= (APOC4-APOC2) ENSP00000467185.1:n.*807T=
ENST00000585786.1:c.24T= (APOC2) ENSP00000465001.1:p.Ala8=
ENST00000589057.5:c.255T= (APOC4-APOC2) ENSP00000468139.1:p.Ala85=
ENST00000590360.2:c.24T= (APOC2) ENSP00000466775.1:p.Ala8=
ENST00000591597.5:c.24T= (APOC2) ENSP00000476835.1:p.Ala8=
ENST00000592257.5:c.24T= (APOC2) ENSP00000477261.1:p.Ala8=
NM_000483.4:c.24T= (APOC2) NP_000474.2:p.Ala8=
NR_037932.1:n.1231T= (APOC4-APOC2)
NM_000483.5:c.24T= (APOC2) MANE Select NP_000474.2:p.Ala8=