Canonical Allele Identifier: CA882680143

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1249764988
• gnomAD v3: 19-44949345-T-C
• gnomAD v4: 19-44949345-T-C
• MyVariant Identifiers: chr19:g.45452602T>C (hg19) ; chr19:g.44949345T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949345T>C , CM000681.2:g.44949345T>C	GRCh38
NC_000019.9:g.45452602T>C , CM000681.1:g.45452602T>C	GRCh37
NC_000019.8:g.50144442T>C	NCBI36
NG_008837.1:g.8360T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.*96T>C (APOC2) MANE Select	ENSP00000252490.5:n.*96T>C
ENST00000252490.5:c.*96T>C (APOC4-APOC2)	ENSP00000252490.4:n.*96T>C
ENST00000585685.5:c.*1185T>C (APOC4-APOC2)	ENSP00000467185.1:n.*1185T>C
ENST00000589057.5:c.*96T>C (APOC4-APOC2)	ENSP00000468139.1:n.*96T>C
ENST00000590360.2:c.*96T>C (APOC2)	ENSP00000466775.1:n.*96T>C
ENST00000591597.5:c.*96T>C (APOC2)	ENSP00000476835.1:n.*96T>C
ENST00000592257.5:c.*196T>C (APOC2)	ENSP00000477261.1:n.*196T>C
NM_000483.4:c.*96T>C (APOC2)	NP_000474.2:n.*96T>C
NR_037932.1:n.1609T>C (APOC4-APOC2)
NM_000483.5:c.*96T>C (APOC2) MANE Select	NP_000474.2:n.*96T>C