Canonical Allele Identifier: CA6289646
Gene: APOC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1936076
ClinVar RCV Id: RCV002642475 RCV003111586
dbSNP Id: rs755061758
ExAC: 11:116701474 C / A
gnomAD v2: 11-116701474-C-A
gnomAD v4: 11-116830758-C-A
MyVariant Identifiers: chr11:g.116701474C>A (hg19) chr11:g.116830758C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830758C>A , CM000673.2:g.116830758C>A GRCh38
NC_000011.9:g.116701474C>A , CM000673.1:g.116701474C>A GRCh37
NC_000011.8:g.116206684C>A NCBI36
NG_008949.1:g.5851C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-15C>A MANE Select ENSP00000227667.2:n.56-15C>A
ENST00000227667.7:c.56-15C>A ENSP00000227667.2:n.56-15C>A
ENST00000375345.3:c.110-15C>A ENSP00000364494.1:n.110-15C>A
ENST00000433777.5:c.56-15C>A ENSP00000410614.1:n.56-15C>A
ENST00000470144.1:n.88-15C>A
ENST00000630701.1:c.110-15C>A ENSP00000486182.1:n.110-15C>A
NM_000040.1:c.56-15C>A NP_000031.1:n.56-15C>A
NM_000040.2:c.56-15C>A NP_000031.1:n.56-15C>A
NM_000040.3:c.56-15C>A MANE Select NP_000031.1:n.56-15C>A
Search 100 bp 5'
Search 100 bp 3'