Canonical Allele Identifier: CA406295398

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452472A>C (hg19) ; chr19:g.44949215A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949215A>C , CM000681.2:g.44949215A>C	GRCh38
NC_000019.9:g.45452472A>C , CM000681.1:g.45452472A>C	GRCh37
NC_000019.8:g.50144312A>C	NCBI36
NG_008837.1:g.8230A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.272A>C (APOC2) MANE Select	ENSP00000252490.5:p.Asp91Ala
ENST00000252490.5:c.272A>C (APOC4-APOC2)	ENSP00000252490.4:p.Asp91Ala
ENST00000585685.5:c.*1055A>C (APOC4-APOC2)	ENSP00000467185.1:n.*1055A>C
ENST00000585786.1:c.*351A>C (APOC2)	ENSP00000465001.1:n.*351A>C
ENST00000589057.5:c.503A>C (APOC4-APOC2)	ENSP00000468139.1:p.Asp168Ala
ENST00000590360.2:c.272A>C (APOC2)	ENSP00000466775.1:p.Asp91Ala
ENST00000591597.5:c.230A>C (APOC2)	ENSP00000476835.1:p.Asp77Ala
ENST00000592257.5:c.*66A>C (APOC2)	ENSP00000477261.1:n.*66A>C
NM_000483.4:c.272A>C (APOC2)	NP_000474.2:p.Asp91Ala
NR_037932.1:n.1479A>C (APOC4-APOC2)
NM_000483.5:c.272A>C (APOC2) MANE Select	NP_000474.2:p.Asp91Ala