Canonical Allele Identifier: CA507796243
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45452497A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949240A>C , CM000681.2:g.44949240A>C GRCh38
NC_000019.9:g.45452497A>C , CM000681.1:g.45452497A>C GRCh37
NC_000019.8:g.50144337A>C NCBI36
NG_008837.1:g.8255A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.297A>C (APOC2) MANE Select ENSP00000252490.5:p.Gly99=
ENST00000252490.5:c.297A>C (APOC4-APOC2) ENSP00000252490.4:p.Gly99=
ENST00000585685.5:c.*1080A>C (APOC4-APOC2) ENSP00000467185.1:n.*1080A>C
ENST00000585786.1:c.*376A>C (APOC2) ENSP00000465001.1:n.*376A>C
ENST00000589057.5:c.528A>C (APOC4-APOC2) ENSP00000468139.1:p.Gly176=
ENST00000590360.2:c.297A>C (APOC2) ENSP00000466775.1:p.Gly99=
ENST00000591597.5:c.255A>C (APOC2) ENSP00000476835.1:p.Gly85=
ENST00000592257.5:c.*91A>C (APOC2) ENSP00000477261.1:n.*91A>C
NM_000483.4:c.297A>C (APOC2) NP_000474.2:p.Gly99=
NR_037932.1:n.1504A>C (APOC4-APOC2)
NM_000483.5:c.297A>C (APOC2) MANE Select NP_000474.2:p.Gly99=
Search 100 bp 5'
Search 100 bp 3'