Canonical Allele Identifier: CA882679811

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1388809874
• MyVariant Identifiers: chr19:g.45451869A>C (hg19) ; chr19:g.44948612A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948612A>C , CM000681.2:g.44948612A>C	GRCh38
NC_000019.9:g.45451869A>C , CM000681.1:g.45451869A>C	GRCh37
NC_000019.8:g.50143709A>C	NCBI36
NG_008837.1:g.7627A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.55+79A>C (APOC2) MANE Select	ENSP00000252490.5:n.55+79A>C
ENST00000252490.5:c.55+79A>C (APOC4-APOC2)	ENSP00000252490.4:n.55+79A>C
ENST00000585685.5:c.*838+79A>C (APOC4-APOC2)	ENSP00000467185.1:n.*838+79A>C
ENST00000585786.1:c.55+79A>C (APOC2)	ENSP00000465001.1:n.55+79A>C
ENST00000589057.5:c.286+79A>C (APOC4-APOC2)	ENSP00000468139.1:n.286+79A>C
ENST00000590360.2:c.55+79A>C (APOC2)	ENSP00000466775.1:n.55+79A>C
ENST00000591597.5:c.55+79A>C (APOC2)	ENSP00000476835.1:n.55+79A>C
ENST00000592257.5:c.55+79A>C (APOC2)	ENSP00000477261.1:n.55+79A>C
NM_000483.4:c.55+79A>C (APOC2)	NP_000474.2:n.55+79A>C
NR_037932.1:n.1262+79A>C (APOC4-APOC2)
NM_000483.5:c.55+79A>C (APOC2) MANE Select	NP_000474.2:n.55+79A>C