Canonical Allele Identifier: CA308875120

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1012101474
• gnomAD v4: 19-44948307-C-G
• MyVariant Identifiers: chr19:g.45451564C>G (hg19) ; chr19:g.44948307C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948307C>G , CM000681.2:g.44948307C>G	GRCh38
NC_000019.9:g.45451564C>G , CM000681.1:g.45451564C>G	GRCh37
NC_000019.8:g.50143404C>G	NCBI36
NG_008837.1:g.7322C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.-13-159C>G (APOC2) MANE Select	ENSP00000252490.5:n.-13-159C>G
ENST00000252490.5:c.-13-159C>G (APOC4-APOC2)	ENSP00000252490.4:n.-13-159C>G
ENST00000585685.5:c.*771-159C>G (APOC4-APOC2)	ENSP00000467185.1:n.*771-159C>G
ENST00000585786.1:c.-172C>G (APOC2)	ENSP00000465001.1:n.-172C>G
ENST00000589057.5:c.219-159C>G (APOC4-APOC2)	ENSP00000468139.1:n.219-159C>G
ENST00000590360.2:c.-13-159C>G (APOC2)	ENSP00000466775.1:n.-13-159C>G
ENST00000591597.5:c.-13-159C>G (APOC2)	ENSP00000476835.1:n.-13-159C>G
ENST00000592257.5:c.-13-159C>G (APOC2)	ENSP00000477261.1:n.-13-159C>G
NM_000483.4:c.-13-159C>G (APOC2)	NP_000474.2:n.-13-159C>G
NR_037932.1:n.1195-159C>G (APOC4-APOC2)
NM_000483.5:c.-13-159C>G (APOC2) MANE Select	NP_000474.2:n.-13-159C>G