Canonical Allele Identifier: CA115626
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2584
ClinVar RCV Id: RCV000002701 RCV000002702
dbSNP Id: rs120074116
MyVariant Identifiers: chr19:g.45452455C>A (hg19) chr19:g.44949198C>A (hg38)
PubMed: PMID:12783430
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949198C>A , CM000681.2:g.44949198C>A GRCh38
NC_000019.9:g.45452455C>A , CM000681.1:g.45452455C>A GRCh37
NC_000019.8:g.50144295C>A NCBI36
NG_008837.1:g.8213C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.255C>A (APOC2) MANE Select ENSP00000252490.5:p.Tyr85Ter
ENST00000252490.5:c.255C>A (APOC4-APOC2) ENSP00000252490.4:p.Tyr85Ter
ENST00000585685.5:c.*1038C>A (APOC4-APOC2) ENSP00000467185.1:n.*1038C>A
ENST00000585786.1:c.*334C>A (APOC2) ENSP00000465001.1:n.*334C>A
ENST00000589057.5:c.486C>A (APOC4-APOC2) ENSP00000468139.1:p.Tyr162Ter
ENST00000590360.2:c.255C>A (APOC2) ENSP00000466775.1:p.Tyr85Ter
ENST00000591597.5:c.213C>A (APOC2) ENSP00000476835.1:p.Tyr71Ter
ENST00000592257.5:c.*49C>A (APOC2) ENSP00000477261.1:n.*49C>A
NM_000483.4:c.255C>A (APOC2) NP_000474.2:p.Tyr85Ter
NR_037932.1:n.1462C>A (APOC4-APOC2)
NM_000483.5:c.255C>A (APOC2) MANE Select NP_000474.2:p.Tyr85Ter
Search 100 bp 5'
Search 100 bp 3'