Canonical Allele Identifier: CA882680025

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1361333147
• MyVariant Identifiers: chr19:g.45452345C>G (hg19) ; chr19:g.44949088C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949088C>G , CM000681.2:g.44949088C>G	GRCh38
NC_000019.9:g.45452345C>G , CM000681.1:g.45452345C>G	GRCh37
NC_000019.8:g.50144185C>G	NCBI36
NG_008837.1:g.8103C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-71C>G (APOC2) MANE Select	ENSP00000252490.5:n.216-71C>G
ENST00000252490.5:c.216-71C>G (APOC4-APOC2)	ENSP00000252490.4:n.216-71C>G
ENST00000585685.5:c.*999-71C>G (APOC4-APOC2)	ENSP00000467185.1:n.*999-71C>G
ENST00000585786.1:c.*224C>G (APOC2)	ENSP00000465001.1:n.*224C>G
ENST00000589057.5:c.447-71C>G (APOC4-APOC2)	ENSP00000468139.1:n.447-71C>G
ENST00000590360.2:c.216-71C>G (APOC2)	ENSP00000466775.1:n.216-71C>G
ENST00000591597.5:c.174-71C>G (APOC2)	ENSP00000476835.1:n.174-71C>G
ENST00000592257.5:c.*10-71C>G (APOC2)	ENSP00000477261.1:n.*10-71C>G
NM_000483.4:c.216-71C>G (APOC2)	NP_000474.2:n.216-71C>G
NR_037932.1:n.1423-71C>G (APOC4-APOC2)
NM_000483.5:c.216-71C>G (APOC2) MANE Select	NP_000474.2:n.216-71C>G