Canonical Allele Identifier: CA996271657

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970356208
• gnomAD v3: 19-44949089-T-C
• gnomAD v4: 19-44949089-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949089T>C , CM000681.2:g.44949089T>C	GRCh38
NC_000019.9:g.45452346T>C , CM000681.1:g.45452346T>C	GRCh37
NC_000019.8:g.50144186T>C	NCBI36
NG_008837.1:g.8104T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.216-70T>C (APOC2) MANE Select	ENSP00000252490.5:n.216-70T>C
ENST00000252490.5:c.216-70T>C (APOC4-APOC2)	ENSP00000252490.4:n.216-70T>C
ENST00000585685.5:c.*999-70T>C (APOC4-APOC2)	ENSP00000467185.1:n.*999-70T>C
ENST00000585786.1:c.*225T>C (APOC2)	ENSP00000465001.1:n.*225T>C
ENST00000589057.5:c.447-70T>C (APOC4-APOC2)	ENSP00000468139.1:n.447-70T>C
ENST00000590360.2:c.216-70T>C (APOC2)	ENSP00000466775.1:n.216-70T>C
ENST00000591597.5:c.174-70T>C (APOC2)	ENSP00000476835.1:n.174-70T>C
ENST00000592257.5:c.*10-70T>C (APOC2)	ENSP00000477261.1:n.*10-70T>C
NM_000483.4:c.216-70T>C (APOC2)	NP_000474.2:n.216-70T>C
NR_037932.1:n.1423-70T>C (APOC4-APOC2)
NM_000483.5:c.216-70T>C (APOC2) MANE Select	NP_000474.2:n.216-70T>C