Canonical Allele Identifier: CA2338188987
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949418G= , CM000681.2:g.44949418G= GRCh38
NC_000019.9:g.45452675G= , CM000681.1:g.45452675G= GRCh37
NC_000019.8:g.50144515G= NCBI36
NG_008837.1:g.8433G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*169G= (APOC2) MANE Select ENSP00000252490.5:n.*169G=
ENST00000252490.5:c.*169G= (APOC4-APOC2) ENSP00000252490.4:n.*169G=
ENST00000585685.5:c.*1258G= (APOC4-APOC2) ENSP00000467185.1:n.*1258G=
ENST00000590360.2:c.*169G= (APOC2) ENSP00000466775.1:n.*169G=
NM_000483.4:c.*169G= (APOC2) NP_000474.2:n.*169G=
NR_037932.1:n.1682G= (APOC4-APOC2)
NM_000483.5:c.*169G= (APOC2) MANE Select NP_000474.2:n.*169G=
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