Canonical Allele Identifier: CA406295335

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs146500837
• MyVariant Identifiers: chr19:g.45452459G>A (hg19) ; chr19:g.44949202G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949202G>A , CM000681.2:g.44949202G>A	GRCh38
NC_000019.9:g.45452459G>A , CM000681.1:g.45452459G>A	GRCh37
NC_000019.8:g.50144299G>A	NCBI36
NG_008837.1:g.8217G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.259G>A (APOC2) MANE Select	ENSP00000252490.5:p.Gly87Ser
ENST00000252490.5:c.259G>A (APOC4-APOC2)	ENSP00000252490.4:p.Gly87Ser
ENST00000585685.5:c.*1042G>A (APOC4-APOC2)	ENSP00000467185.1:n.*1042G>A
ENST00000585786.1:c.*338G>A (APOC2)	ENSP00000465001.1:n.*338G>A
ENST00000589057.5:c.490G>A (APOC4-APOC2)	ENSP00000468139.1:p.Gly164Ser
ENST00000590360.2:c.259G>A (APOC2)	ENSP00000466775.1:p.Gly87Ser
ENST00000591597.5:c.217G>A (APOC2)	ENSP00000476835.1:p.Gly73Ser
ENST00000592257.5:c.*53G>A (APOC2)	ENSP00000477261.1:n.*53G>A
NM_000483.4:c.259G>A (APOC2)	NP_000474.2:p.Gly87Ser
NR_037932.1:n.1466G>A (APOC4-APOC2)
NM_000483.5:c.259G>A (APOC2) MANE Select	NP_000474.2:p.Gly87Ser