Canonical Allele Identifier: CA2576663988
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949345T>G , CM000681.2:g.44949345T>G GRCh38
NC_000019.9:g.45452602T>G , CM000681.1:g.45452602T>G GRCh37
NC_000019.8:g.50144442T>G NCBI36
NG_008837.1:g.8360T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*96T>G (APOC2) MANE Select ENSP00000252490.5:n.*96T>G
ENST00000252490.5:c.*96T>G (APOC4-APOC2) ENSP00000252490.4:n.*96T>G
ENST00000585685.5:c.*1185T>G (APOC4-APOC2) ENSP00000467185.1:n.*1185T>G
ENST00000589057.5:c.*96T>G (APOC4-APOC2) ENSP00000468139.1:n.*96T>G
ENST00000590360.2:c.*96T>G (APOC2) ENSP00000466775.1:n.*96T>G
ENST00000591597.5:c.*96T>G (APOC2) ENSP00000476835.1:n.*96T>G
ENST00000592257.5:c.*196T>G (APOC2) ENSP00000477261.1:n.*196T>G
NM_000483.4:c.*96T>G (APOC2) NP_000474.2:n.*96T>G
NR_037932.1:n.1609T>G (APOC4-APOC2)
NM_000483.5:c.*96T>G (APOC2) MANE Select NP_000474.2:n.*96T>G
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