Canonical Allele Identifier: CA942608806

Gene: APOC3

Linked Data

• dbSNP Id: rs1941478635
• gnomAD v3: 11-116832911-C-T
• gnomAD v4: 11-116832911-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832911C>T , CM000673.2:g.116832911C>T	GRCh38
NC_000011.9:g.116703627C>T , CM000673.1:g.116703627C>T	GRCh37
NC_000011.8:g.116208837C>T	NCBI36
NG_008949.1:g.8004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.*27C>T MANE Select	ENSP00000227667.2:n.*27C>T
ENST00000227667.7:c.*27C>T	ENSP00000227667.2:n.*27C>T
ENST00000375345.3:c.*27C>T	ENSP00000364494.1:n.*27C>T
ENST00000630701.1:c.381C>T	ENSP00000486182.1:n.381C>T
NM_000040.1:c.*27C>T	NP_000031.1:n.*27C>T
NM_000040.2:c.*27C>T	NP_000031.1:n.*27C>T
NM_000040.3:c.*27C>T MANE Select	NP_000031.1:n.*27C>T