Canonical Allele Identifier: CA507796203
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45452440A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949183A>G , CM000681.2:g.44949183A>G GRCh38
NC_000019.9:g.45452440A>G , CM000681.1:g.45452440A>G GRCh37
NC_000019.8:g.50144280A>G NCBI36
NG_008837.1:g.8198A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.240A>G (APOC2) MANE Select ENSP00000252490.5:p.Ala80=
ENST00000252490.5:c.240A>G (APOC4-APOC2) ENSP00000252490.4:p.Ala80=
ENST00000585685.5:c.*1023A>G (APOC4-APOC2) ENSP00000467185.1:n.*1023A>G
ENST00000585786.1:c.*319A>G (APOC2) ENSP00000465001.1:n.*319A>G
ENST00000589057.5:c.471A>G (APOC4-APOC2) ENSP00000468139.1:p.Ala157=
ENST00000590360.2:c.240A>G (APOC2) ENSP00000466775.1:p.Ala80=
ENST00000591597.5:c.198A>G (APOC2) ENSP00000476835.1:p.Ala66=
ENST00000592257.5:c.*34A>G (APOC2) ENSP00000477261.1:n.*34A>G
NM_000483.4:c.240A>G (APOC2) NP_000474.2:p.Ala80=
NR_037932.1:n.1447A>G (APOC4-APOC2)
NM_000483.5:c.240A>G (APOC2) MANE Select NP_000474.2:p.Ala80=