Canonical Allele Identifier: CA2585725176
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

gnomAD v4: 19-44949414-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949414C>G , CM000681.2:g.44949414C>G GRCh38
NC_000019.9:g.45452671C>G , CM000681.1:g.45452671C>G GRCh37
NC_000019.8:g.50144511C>G NCBI36
NG_008837.1:g.8429C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*165C>G (APOC2) MANE Select ENSP00000252490.5:n.*165C>G
ENST00000252490.5:c.*165C>G (APOC4-APOC2) ENSP00000252490.4:n.*165C>G
ENST00000585685.5:c.*1254C>G (APOC4-APOC2) ENSP00000467185.1:n.*1254C>G
ENST00000590360.2:c.*165C>G (APOC2) ENSP00000466775.1:n.*165C>G
NM_000483.4:c.*165C>G (APOC2) NP_000474.2:n.*165C>G
NR_037932.1:n.1678C>G (APOC4-APOC2)
NM_000483.5:c.*165C>G (APOC2) MANE Select NP_000474.2:n.*165C>G
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