Canonical Allele Identifier: CA308876529

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs201322649
• MyVariant Identifiers: chr19:g.45452692_45452693insG (hg19) ; chr19:g.44949435_44949436insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949438dup , CM000681.2:g.44949438dup	GRCh38
NC_000019.9:g.45452695dup , CM000681.1:g.45452695dup	GRCh37
NC_000019.8:g.50144535dup	NCBI36
NG_008837.1:g.8453dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.*189dup (APOC2) MANE Select	ENSP00000252490.5:n.*189dup
ENST00000252490.5:c.*189dup (APOC4-APOC2)	ENSP00000252490.4:n.*189dup
ENST00000585685.5:c.*1278dup (APOC4-APOC2)	ENSP00000467185.1:n.*1278dup
ENST00000590360.2:c.*189dup (APOC2)	ENSP00000466775.1:n.*189dup
NM_000483.4:c.*189dup (APOC2)	NP_000474.2:n.*189dup
NR_037932.1:n.1702dup (APOC4-APOC2)
NM_000483.5:c.*189dup (APOC2) MANE Select	NP_000474.2:n.*189dup