Canonical Allele Identifier: CA308874945
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs555315266
gnomAD v2: 19-45451335-G-A
gnomAD v3: 19-44948078-G-A
gnomAD v4: 19-44948078-G-A
MyVariant Identifiers: chr19:g.45451335G>A (hg19) chr19:g.44948078G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948078G>A , CM000681.2:g.44948078G>A GRCh38
NC_000019.9:g.45451335G>A , CM000681.1:g.45451335G>A GRCh37
NC_000019.8:g.50143175G>A NCBI36
NG_008837.1:g.7093G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.-13-388G>A (APOC2) MANE Select ENSP00000252490.5:n.-13-388G>A
ENST00000252490.5:c.-13-388G>A (APOC4-APOC2) ENSP00000252490.4:n.-13-388G>A
ENST00000585685.5:c.*771-388G>A (APOC4-APOC2) ENSP00000467185.1:n.*771-388G>A
ENST00000589057.5:c.219-388G>A (APOC4-APOC2) ENSP00000468139.1:n.219-388G>A
ENST00000590360.2:c.-13-388G>A (APOC2) ENSP00000466775.1:n.-13-388G>A
ENST00000591597.5:c.-13-388G>A (APOC2) ENSP00000476835.1:n.-13-388G>A
ENST00000592257.5:c.-13-388G>A (APOC2) ENSP00000477261.1:n.-13-388G>A
NM_000483.4:c.-13-388G>A (APOC2) NP_000474.2:n.-13-388G>A
NR_037932.1:n.1195-388G>A (APOC4-APOC2)
NM_000483.5:c.-13-388G>A (APOC2) MANE Select NP_000474.2:n.-13-388G>A
Search 100 bp 5'
Search 100 bp 3'