Canonical Allele Identifier: CA406291330

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1568634542
• MyVariant Identifiers: chr19:g.45451723G>A (hg19) ; chr19:g.44948466G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948466G>A , CM000681.2:g.44948466G>A	GRCh38
NC_000019.9:g.45451723G>A , CM000681.1:g.45451723G>A	GRCh37
NC_000019.8:g.50143563G>A	NCBI36
NG_008837.1:g.7481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13G>A (APOC2) MANE Select	ENSP00000252490.5:n.-13G>A
ENST00000252490.5:c.-13G>A (APOC4-APOC2)	ENSP00000252490.4:n.-13G>A
ENST00000585685.5:c.*771G>A (APOC4-APOC2)	ENSP00000467185.1:n.*771G>A
ENST00000585786.1:c.-13G>A (APOC2)	ENSP00000465001.1:n.-13G>A
ENST00000589057.5:c.219G>A (APOC4-APOC2)	ENSP00000468139.1:p.Trp73Ter
ENST00000590360.2:c.-13G>A (APOC2)	ENSP00000466775.1:n.-13G>A
ENST00000591597.5:c.-13G>A (APOC2)	ENSP00000476835.1:n.-13G>A
ENST00000592257.5:c.-13G>A (APOC2)	ENSP00000477261.1:n.-13G>A
NM_000483.4:c.-13G>A (APOC2)	NP_000474.2:n.-13G>A
NR_037932.1:n.1195G>A (APOC4-APOC2)
NM_000483.5:c.-13G>A (APOC2) MANE Select	NP_000474.2:n.-13G>A