Canonical Allele Identifier: CA507796221

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452470T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949213T>A , CM000681.2:g.44949213T>A	GRCh38
NC_000019.9:g.45452470T>A , CM000681.1:g.45452470T>A	GRCh37
NC_000019.8:g.50144310T>A	NCBI36
NG_008837.1:g.8228T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.270T>A (APOC2) MANE Select	ENSP00000252490.5:p.Thr90=
ENST00000252490.5:c.270T>A (APOC4-APOC2)	ENSP00000252490.4:p.Thr90=
ENST00000585685.5:c.*1053T>A (APOC4-APOC2)	ENSP00000467185.1:n.*1053T>A
ENST00000585786.1:c.*349T>A (APOC2)	ENSP00000465001.1:n.*349T>A
ENST00000589057.5:c.501T>A (APOC4-APOC2)	ENSP00000468139.1:p.Thr167=
ENST00000590360.2:c.270T>A (APOC2)	ENSP00000466775.1:p.Thr90=
ENST00000591597.5:c.228T>A (APOC2)	ENSP00000476835.1:p.Thr76=
ENST00000592257.5:c.*64T>A (APOC2)	ENSP00000477261.1:n.*64T>A
NM_000483.4:c.270T>A (APOC2)	NP_000474.2:p.Thr90=
NR_037932.1:n.1477T>A (APOC4-APOC2)
NM_000483.5:c.270T>A (APOC2) MANE Select	NP_000474.2:p.Thr90=