Canonical Allele Identifier: CA406295439
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45452480C>G (hg19) chr19:g.44949223C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949223C>G , CM000681.2:g.44949223C>G GRCh38
NC_000019.9:g.45452480C>G , CM000681.1:g.45452480C>G GRCh37
NC_000019.8:g.50144320C>G NCBI36
NG_008837.1:g.8238C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.280C>G (APOC2) MANE Select ENSP00000252490.5:p.Leu94Val
ENST00000252490.5:c.280C>G (APOC4-APOC2) ENSP00000252490.4:p.Leu94Val
ENST00000585685.5:c.*1063C>G (APOC4-APOC2) ENSP00000467185.1:n.*1063C>G
ENST00000585786.1:c.*359C>G (APOC2) ENSP00000465001.1:n.*359C>G
ENST00000589057.5:c.511C>G (APOC4-APOC2) ENSP00000468139.1:p.Leu171Val
ENST00000590360.2:c.280C>G (APOC2) ENSP00000466775.1:p.Leu94Val
ENST00000591597.5:c.238C>G (APOC2) ENSP00000476835.1:p.Leu80Val
ENST00000592257.5:c.*74C>G (APOC2) ENSP00000477261.1:n.*74C>G
NM_000483.4:c.280C>G (APOC2) NP_000474.2:p.Leu94Val
NR_037932.1:n.1487C>G (APOC4-APOC2)
NM_000483.5:c.280C>G (APOC2) MANE Select NP_000474.2:p.Leu94Val
Search 100 bp 5'
Search 100 bp 3'