Canonical Allele Identifier: CA476868976

Gene: APOC3

Linked Data

• dbSNP Id: rs1941478089
• gnomAD v3: 11-116832875-G-A
• gnomAD v4: 11-116832875-G-A
• MyVariant Identifiers: chr11:g.116703591G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832875G>A , CM000673.2:g.116832875G>A	GRCh38
NC_000011.9:g.116703591G>A , CM000673.1:g.116703591G>A	GRCh37
NC_000011.8:g.116208801G>A	NCBI36
NG_008949.1:g.7968G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.291G>A MANE Select	ENSP00000227667.2:p.Val97=
ENST00000227667.7:c.291G>A	ENSP00000227667.2:p.Val97=
ENST00000375345.3:c.345G>A	ENSP00000364494.1:p.Val115=
ENST00000630701.1:c.345G>A	ENSP00000486182.1:p.Val115=
NM_000040.1:c.291G>A	NP_000031.1:p.Val97=
NM_000040.2:c.291G>A	NP_000031.1:p.Val97=
NM_000040.3:c.291G>A MANE Select	NP_000031.1:p.Val97=