Canonical Allele Identifier: CA2338188986
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949416C= , CM000681.2:g.44949416C= GRCh38
NC_000019.9:g.45452673C= , CM000681.1:g.45452673C= GRCh37
NC_000019.8:g.50144513C= NCBI36
NG_008837.1:g.8431C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*167C= (APOC2) MANE Select ENSP00000252490.5:n.*167C=
ENST00000252490.5:c.*167C= (APOC4-APOC2) ENSP00000252490.4:n.*167C=
ENST00000585685.5:c.*1256C= (APOC4-APOC2) ENSP00000467185.1:n.*1256C=
ENST00000590360.2:c.*167C= (APOC2) ENSP00000466775.1:n.*167C=
NM_000483.4:c.*167C= (APOC2) NP_000474.2:n.*167C=
NR_037932.1:n.1680C= (APOC4-APOC2)
NM_000483.5:c.*167C= (APOC2) MANE Select NP_000474.2:n.*167C=
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