Canonical Allele Identifier: CA406294869

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452114T>G (hg19) ; chr19:g.44948857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948857T>G , CM000681.2:g.44948857T>G	GRCh38
NC_000019.9:g.45452114T>G , CM000681.1:g.45452114T>G	GRCh37
NC_000019.8:g.50143954T>G	NCBI36
NG_008837.1:g.7872T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.212T>G (APOC2) MANE Select	ENSP00000252490.5:p.Leu71Arg
ENST00000252490.5:c.212T>G (APOC4-APOC2)	ENSP00000252490.4:p.Leu71Arg
ENST00000585685.5:c.*995T>G (APOC4-APOC2)	ENSP00000467185.1:n.*995T>G
ENST00000585786.1:c.212T>G (APOC2)	ENSP00000465001.1:p.Leu71Arg
ENST00000589057.5:c.443T>G (APOC4-APOC2)	ENSP00000468139.1:p.Leu148Arg
ENST00000590360.2:c.212T>G (APOC2)	ENSP00000466775.1:p.Leu71Arg
ENST00000591597.5:c.173+39T>G (APOC2)	ENSP00000476835.1:n.173+39T>G
ENST00000592257.5:c.*6T>G (APOC2)	ENSP00000477261.1:n.*6T>G
NM_000483.4:c.212T>G (APOC2)	NP_000474.2:p.Leu71Arg
NR_037932.1:n.1419T>G (APOC4-APOC2)
NM_000483.5:c.212T>G (APOC2) MANE Select	NP_000474.2:p.Leu71Arg