Canonical Allele Identifier: CA10642918
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329461
ClinVar RCV Id: RCV000282845
dbSNP Id: rs886054487
gnomAD v3: 19-44949452-G-A
gnomAD v4: 19-44949452-G-A
MyVariant Identifiers: chr19:g.45452709G>A (hg19) chr19:g.44949452G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949452G>A , CM000681.2:g.44949452G>A GRCh38
NC_000019.9:g.45452709G>A , CM000681.1:g.45452709G>A GRCh37
NC_000019.8:g.50144549G>A NCBI36
NG_008837.1:g.8467G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*203G>A (APOC2) MANE Select ENSP00000252490.5:n.*203G>A
ENST00000252490.5:c.*203G>A (APOC4-APOC2) ENSP00000252490.4:n.*203G>A
ENST00000585685.5:c.*1292G>A (APOC4-APOC2) ENSP00000467185.1:n.*1292G>A
ENST00000590360.2:c.*203G>A (APOC2) ENSP00000466775.1:n.*203G>A
NM_000483.4:c.*203G>A (APOC2) NP_000474.2:n.*203G>A
NR_037932.1:n.1716G>A (APOC4-APOC2)
NM_000483.5:c.*203G>A (APOC2) MANE Select NP_000474.2:n.*203G>A
Search 100 bp 5'
Search 100 bp 3'