Canonical Allele Identifier: CA996271405

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1249002250
• gnomAD v3: 19-44948978-T-A
• gnomAD v4: 19-44948978-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948978T>A , CM000681.2:g.44948978T>A	GRCh38
NC_000019.9:g.45452235T>A , CM000681.1:g.45452235T>A	GRCh37
NC_000019.8:g.50144075T>A	NCBI36
NG_008837.1:g.7993T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+118T>A (APOC2) MANE Select	ENSP00000252490.5:n.215+118T>A
ENST00000252490.5:c.215+118T>A (APOC4-APOC2)	ENSP00000252490.4:n.215+118T>A
ENST00000585685.5:c.*998+118T>A (APOC4-APOC2)	ENSP00000467185.1:n.*998+118T>A
ENST00000585786.1:c.*114T>A (APOC2)	ENSP00000465001.1:n.*114T>A
ENST00000589057.5:c.446+118T>A (APOC4-APOC2)	ENSP00000468139.1:n.446+118T>A
ENST00000590360.2:c.215+118T>A (APOC2)	ENSP00000466775.1:n.215+118T>A
ENST00000591597.5:c.173+160T>A (APOC2)	ENSP00000476835.1:n.173+160T>A
ENST00000592257.5:c.*9+118T>A (APOC2)	ENSP00000477261.1:n.*9+118T>A
NM_000483.4:c.215+118T>A (APOC2)	NP_000474.2:n.215+118T>A
NR_037932.1:n.1422+118T>A (APOC4-APOC2)
NM_000483.5:c.215+118T>A (APOC2) MANE Select	NP_000474.2:n.215+118T>A