Canonical Allele Identifier: CA2338188680
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948839C= , CM000681.2:g.44948839C= GRCh38
NC_000019.9:g.45452096C= , CM000681.1:g.45452096C= GRCh37
NC_000019.8:g.50143936C= NCBI36
NG_008837.1:g.7854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.194C= (APOC2) MANE Select ENSP00000252490.5:p.Pro65=
ENST00000252490.5:c.194C= (APOC4-APOC2) ENSP00000252490.4:p.Pro65=
ENST00000585685.5:c.*977C= (APOC4-APOC2) ENSP00000467185.1:n.*977C=
ENST00000585786.1:c.194C= (APOC2) ENSP00000465001.1:p.Pro65=
ENST00000589057.5:c.425C= (APOC4-APOC2) ENSP00000468139.1:p.Pro142=
ENST00000590360.2:c.194C= (APOC2) ENSP00000466775.1:p.Pro65=
ENST00000591597.5:c.173+21C= (APOC2) ENSP00000476835.1:n.173+21C=
ENST00000592257.5:c.132C= (APOC2) ENSP00000477261.1:p.Ala44=
NM_000483.4:c.194C= (APOC2) NP_000474.2:p.Pro65=
NR_037932.1:n.1401C= (APOC4-APOC2)
NM_000483.5:c.194C= (APOC2) MANE Select NP_000474.2:p.Pro65=