Canonical Allele Identifier: CA406291474

Gene: APOC2 APOC4-APOC2

Linked Data

• ClinVar Variation Id: 1744708
• ClinVar RCV Id: RCV002343058
• gnomAD v4: 19-44948482-G-C
• MyVariant Identifiers: chr19:g.45451739G>C (hg19) ; chr19:g.44948482G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948482G>C , CM000681.2:g.44948482G>C	GRCh38
NC_000019.9:g.45451739G>C , CM000681.1:g.45451739G>C	GRCh37
NC_000019.8:g.50143579G>C	NCBI36
NG_008837.1:g.7497G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.4G>C (APOC2) MANE Select	ENSP00000252490.5:p.Gly2Arg
ENST00000252490.5:c.4G>C (APOC4-APOC2)	ENSP00000252490.4:p.Gly2Arg
ENST00000585685.5:c.*787G>C (APOC4-APOC2)	ENSP00000467185.1:n.*787G>C
ENST00000585786.1:c.4G>C (APOC2)	ENSP00000465001.1:p.Gly2Arg
ENST00000589057.5:c.235G>C (APOC4-APOC2)	ENSP00000468139.1:p.Gly79Arg
ENST00000590360.2:c.4G>C (APOC2)	ENSP00000466775.1:p.Gly2Arg
ENST00000591597.5:c.4G>C (APOC2)	ENSP00000476835.1:p.Gly2Arg
ENST00000592257.5:c.4G>C (APOC2)	ENSP00000477261.1:p.Gly2Arg
NM_000483.4:c.4G>C (APOC2)	NP_000474.2:p.Gly2Arg
NR_037932.1:n.1211G>C (APOC4-APOC2)
NM_000483.5:c.4G>C (APOC2) MANE Select	NP_000474.2:p.Gly2Arg