Canonical Allele Identifier: CA2338188631
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948486C= , CM000681.2:g.44948486C= GRCh38
NC_000019.9:g.45451743C= , CM000681.1:g.45451743C= GRCh37
NC_000019.8:g.50143583C= NCBI36
NG_008837.1:g.7501C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.8C= (APOC2) MANE Select ENSP00000252490.5:p.Thr3=
ENST00000252490.5:c.8C= (APOC4-APOC2) ENSP00000252490.4:p.Thr3=
ENST00000585685.5:c.*791C= (APOC4-APOC2) ENSP00000467185.1:n.*791C=
ENST00000585786.1:c.8C= (APOC2) ENSP00000465001.1:p.Thr3=
ENST00000589057.5:c.239C= (APOC4-APOC2) ENSP00000468139.1:p.Thr80=
ENST00000590360.2:c.8C= (APOC2) ENSP00000466775.1:p.Thr3=
ENST00000591597.5:c.8C= (APOC2) ENSP00000476835.1:p.Thr3=
ENST00000592257.5:c.8C= (APOC2) ENSP00000477261.1:p.Thr3=
NM_000483.4:c.8C= (APOC2) NP_000474.2:p.Thr3=
NR_037932.1:n.1215C= (APOC4-APOC2)
NM_000483.5:c.8C= (APOC2) MANE Select NP_000474.2:p.Thr3=