Canonical Allele Identifier: CA507796230

Gene: APOC2 APOC4-APOC2

Linked Data

• ClinVar Variation Id: 1796580
• ClinVar RCV Id: RCV002435111
• MyVariant Identifiers: chr19:g.45452482T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949225T>C , CM000681.2:g.44949225T>C	GRCh38
NC_000019.9:g.45452482T>C , CM000681.1:g.45452482T>C	GRCh37
NC_000019.8:g.50144322T>C	NCBI36
NG_008837.1:g.8240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.282T>C (APOC2) MANE Select	ENSP00000252490.5:p.Leu94=
ENST00000252490.5:c.282T>C (APOC4-APOC2)	ENSP00000252490.4:p.Leu94=
ENST00000585685.5:c.*1065T>C (APOC4-APOC2)	ENSP00000467185.1:n.*1065T>C
ENST00000585786.1:c.*361T>C (APOC2)	ENSP00000465001.1:n.*361T>C
ENST00000589057.5:c.513T>C (APOC4-APOC2)	ENSP00000468139.1:p.Leu171=
ENST00000590360.2:c.282T>C (APOC2)	ENSP00000466775.1:p.Leu94=
ENST00000591597.5:c.240T>C (APOC2)	ENSP00000476835.1:p.Leu80=
ENST00000592257.5:c.*76T>C (APOC2)	ENSP00000477261.1:n.*76T>C
NM_000483.4:c.282T>C (APOC2)	NP_000474.2:p.Leu94=
NR_037932.1:n.1489T>C (APOC4-APOC2)
NM_000483.5:c.282T>C (APOC2) MANE Select	NP_000474.2:p.Leu94=