Canonical Allele Identifier: CA308876494

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs35699384
• MyVariant Identifiers: chr19:g.45452676_45452677insT (hg19) ; chr19:g.44949419_44949420insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949423dup , CM000681.2:g.44949423dup	GRCh38
NC_000019.9:g.45452680dup , CM000681.1:g.45452680dup	GRCh37
NC_000019.8:g.50144520dup	NCBI36
NG_008837.1:g.8438dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.*174dup (APOC2) MANE Select	ENSP00000252490.5:n.*174dup
ENST00000252490.5:c.*174dup (APOC4-APOC2)	ENSP00000252490.4:n.*174dup
ENST00000585685.5:c.*1263dup (APOC4-APOC2)	ENSP00000467185.1:n.*1263dup
ENST00000590360.2:c.*174dup (APOC2)	ENSP00000466775.1:n.*174dup
NM_000483.4:c.*174dup (APOC2)	NP_000474.2:n.*174dup
NR_037932.1:n.1687dup (APOC4-APOC2)
NM_000483.5:c.*174dup (APOC2) MANE Select	NP_000474.2:n.*174dup