Canonical Allele Identifier: CA882679820

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1279646391
• MyVariant Identifiers: chr19:g.45451925C>T (hg19) ; chr19:g.44948668C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948668C>T , CM000681.2:g.44948668C>T	GRCh38
NC_000019.9:g.45451925C>T , CM000681.1:g.45451925C>T	GRCh37
NC_000019.8:g.50143765C>T	NCBI36
NG_008837.1:g.7683C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.56-33C>T (APOC2) MANE Select	ENSP00000252490.5:n.56-33C>T
ENST00000252490.5:c.56-33C>T (APOC4-APOC2)	ENSP00000252490.4:n.56-33C>T
ENST00000585685.5:c.*839-33C>T (APOC4-APOC2)	ENSP00000467185.1:n.*839-33C>T
ENST00000585786.1:c.56-33C>T (APOC2)	ENSP00000465001.1:n.56-33C>T
ENST00000589057.5:c.287-33C>T (APOC4-APOC2)	ENSP00000468139.1:n.287-33C>T
ENST00000590360.2:c.56-33C>T (APOC2)	ENSP00000466775.1:n.56-33C>T
ENST00000591597.5:c.56-33C>T (APOC2)	ENSP00000476835.1:n.56-33C>T
ENST00000592257.5:c.56-95C>T (APOC2)	ENSP00000477261.1:n.56-95C>T
NM_000483.4:c.56-33C>T (APOC2)	NP_000474.2:n.56-33C>T
NR_037932.1:n.1263-33C>T (APOC4-APOC2)
NM_000483.5:c.56-33C>T (APOC2) MANE Select	NP_000474.2:n.56-33C>T