Canonical Allele Identifier: CA507795961
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970347000
MyVariant Identifiers: chr19:g.45451753C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948496C>A , CM000681.2:g.44948496C>A GRCh38
NC_000019.9:g.45451753C>A , CM000681.1:g.45451753C>A GRCh37
NC_000019.8:g.50143593C>A NCBI36
NG_008837.1:g.7511C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.18C>A (APOC2) MANE Select ENSP00000252490.5:p.Leu6=
ENST00000252490.5:c.18C>A (APOC4-APOC2) ENSP00000252490.4:p.Leu6=
ENST00000585685.5:c.*801C>A (APOC4-APOC2) ENSP00000467185.1:n.*801C>A
ENST00000585786.1:c.18C>A (APOC2) ENSP00000465001.1:p.Leu6=
ENST00000589057.5:c.249C>A (APOC4-APOC2) ENSP00000468139.1:p.Leu83=
ENST00000590360.2:c.18C>A (APOC2) ENSP00000466775.1:p.Leu6=
ENST00000591597.5:c.18C>A (APOC2) ENSP00000476835.1:p.Leu6=
ENST00000592257.5:c.18C>A (APOC2) ENSP00000477261.1:p.Leu6=
NM_000483.4:c.18C>A (APOC2) NP_000474.2:p.Leu6=
NR_037932.1:n.1225C>A (APOC4-APOC2)
NM_000483.5:c.18C>A (APOC2) MANE Select NP_000474.2:p.Leu6=