Canonical Allele Identifier: CA308875497
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs370703931

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948550G>A , CM000681.2:g.44948550G>A GRCh38
NC_000019.9:g.45451807G>A , CM000681.1:g.45451807G>A GRCh37
NC_000019.8:g.50143647G>A NCBI36
NG_008837.1:g.7565G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.55+17G>A (APOC2) MANE Select ENSP00000252490.5:n.55+17G>A
ENST00000252490.5:c.55+17G>A (APOC4-APOC2) ENSP00000252490.4:n.55+17G>A
ENST00000585685.5:c.*838+17G>A (APOC4-APOC2) ENSP00000467185.1:n.*838+17G>A
ENST00000585786.1:c.55+17G>A (APOC2) ENSP00000465001.1:n.55+17G>A
ENST00000589057.5:c.286+17G>A (APOC4-APOC2) ENSP00000468139.1:n.286+17G>A
ENST00000590360.2:c.55+17G>A (APOC2) ENSP00000466775.1:n.55+17G>A
ENST00000591597.5:c.55+17G>A (APOC2) ENSP00000476835.1:n.55+17G>A
ENST00000592257.5:c.55+17G>A (APOC2) ENSP00000477261.1:n.55+17G>A
NM_000483.4:c.55+17G>A (APOC2) NP_000474.2:n.55+17G>A
NR_037932.1:n.1262+17G>A (APOC4-APOC2)
NM_000483.5:c.55+17G>A (APOC2) MANE Select NP_000474.2:n.55+17G>A