Canonical Allele Identifier: CA229321277

Gene: APOC3

Linked Data

• dbSNP Id: rs964270062
• gnomAD v2: 11-116703789-GT-G
• gnomAD v3: 11-116833073-GT-G
• gnomAD v4: 11-116833073-GT-G
• MyVariant Identifiers: chr11:g.116703790del (hg19) ; chr11:g.116833074del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116833074del , CM000673.2:g.116833074del	GRCh38
NC_000011.9:g.116703790del , CM000673.1:g.116703790del	GRCh37
NC_000011.8:g.116209000del	NCBI36
NG_008949.1:g.8167del

Transcript Alleles

HGVS	Amino-acid Change
NM_000040.2:c.*190del	NP_000031.1:n.*190del