Canonical Allele Identifier: CA115618
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579
dbSNP Id: rs120074112

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948479A>G , CM000681.2:g.44948479A>G GRCh38
NC_000019.9:g.45451736A>G , CM000681.1:g.45451736A>G GRCh37
NC_000019.8:g.50143576A>G NCBI36
NG_008837.1:g.7494A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.1A>G
ENST00000252490.5:c.1A>G
ENST00000585685.5:c.*784A>G ENSP00000467185.1:p.=
ENST00000585786.1:c.1A>G
ENST00000589057.5:c.232A>G ENSP00000468139.1:p.Met78Val
ENST00000590360.2:c.1A>G
ENST00000591597.5:c.1A>G
ENST00000592257.5:c.1A>G
NM_000483.4:c.1A>G (APOC2)
NR_037932.1:n.1208A>G (APOC4-APOC2)
NM_000483.5:c.1A>G (APOC2)