Canonical Allele Identifier: CA2576663987
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949343C>G , CM000681.2:g.44949343C>G GRCh38
NC_000019.9:g.45452600C>G , CM000681.1:g.45452600C>G GRCh37
NC_000019.8:g.50144440C>G NCBI36
NG_008837.1:g.8358C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*94C>G (APOC2) MANE Select ENSP00000252490.5:n.*94C>G
ENST00000252490.5:c.*94C>G (APOC4-APOC2) ENSP00000252490.4:n.*94C>G
ENST00000585685.5:c.*1183C>G (APOC4-APOC2) ENSP00000467185.1:n.*1183C>G
ENST00000589057.5:c.*94C>G (APOC4-APOC2) ENSP00000468139.1:n.*94C>G
ENST00000590360.2:c.*94C>G (APOC2) ENSP00000466775.1:n.*94C>G
ENST00000591597.5:c.*94C>G (APOC2) ENSP00000476835.1:n.*94C>G
ENST00000592257.5:c.*194C>G (APOC2) ENSP00000477261.1:n.*194C>G
NM_000483.4:c.*94C>G (APOC2) NP_000474.2:n.*94C>G
NR_037932.1:n.1607C>G (APOC4-APOC2)
NM_000483.5:c.*94C>G (APOC2) MANE Select NP_000474.2:n.*94C>G
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