Canonical Allele Identifier: CA2338188318
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948119C= , CM000681.2:g.44948119C= GRCh38
NC_000019.9:g.45451376C= , CM000681.1:g.45451376C= GRCh37
NC_000019.8:g.50143216C= NCBI36
NG_008837.1:g.7134C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.-13-347C= (APOC2) MANE Select ENSP00000252490.5:n.-13-347C=
ENST00000252490.5:c.-13-347C= (APOC4-APOC2) ENSP00000252490.4:n.-13-347C=
ENST00000585685.5:c.*771-347C= (APOC4-APOC2) ENSP00000467185.1:n.*771-347C=
ENST00000589057.5:c.219-347C= (APOC4-APOC2) ENSP00000468139.1:n.219-347C=
ENST00000590360.2:c.-13-347C= (APOC2) ENSP00000466775.1:n.-13-347C=
ENST00000591597.5:c.-13-347C= (APOC2) ENSP00000476835.1:n.-13-347C=
ENST00000592257.5:c.-13-347C= (APOC2) ENSP00000477261.1:n.-13-347C=
NM_000483.4:c.-13-347C= (APOC2) NP_000474.2:n.-13-347C=
NR_037932.1:n.1195-347C= (APOC4-APOC2)
NM_000483.5:c.-13-347C= (APOC2) MANE Select NP_000474.2:n.-13-347C=