Canonical Allele Identifier: CA6289707
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs781170854
ExAC: 11:116703589 G / A
gnomAD v2: 11-116703589-G-A
gnomAD v3: 11-116832873-G-A
gnomAD v4: 11-116832873-G-A
MyVariant Identifiers: chr11:g.116703589G>A (hg19) chr11:g.116832873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832873G>A , CM000673.2:g.116832873G>A GRCh38
NC_000011.9:g.116703589G>A , CM000673.1:g.116703589G>A GRCh37
NC_000011.8:g.116208799G>A NCBI36
NG_008949.1:g.7966G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.289G>A MANE Select ENSP00000227667.2:p.Val97Met
ENST00000227667.7:c.289G>A ENSP00000227667.2:p.Val97Met
ENST00000375345.3:c.343G>A ENSP00000364494.1:p.Val115Met
ENST00000630701.1:c.343G>A ENSP00000486182.1:p.Val115Met
NM_000040.1:c.289G>A NP_000031.1:p.Val97Met
NM_000040.2:c.289G>A NP_000031.1:p.Val97Met
NM_000040.3:c.289G>A MANE Select NP_000031.1:p.Val97Met
Search 100 bp 5'
Search 100 bp 3'