Canonical Allele Identifier: CA942608842
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941480432
gnomAD v3: 11-116833054-G-A
gnomAD v4: 11-116833054-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833054G>A , CM000673.2:g.116833054G>A GRCh38
NC_000011.9:g.116703770G>A , CM000673.1:g.116703770G>A GRCh37
NC_000011.8:g.116208980G>A NCBI36
NG_008949.1:g.8147G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*170G>A MANE Select ENSP00000227667.2:n.*170G>A
ENST00000227667.7:c.*170G>A ENSP00000227667.2:n.*170G>A
ENST00000375345.3:c.*170G>A ENSP00000364494.1:n.*170G>A
ENST00000630701.1:c.524G>A ENSP00000486182.1:n.524G>A
NM_000040.1:c.*170G>A NP_000031.1:n.*170G>A
NM_000040.2:c.*170G>A NP_000031.1:n.*170G>A
NM_000040.3:c.*170G>A MANE Select NP_000031.1:n.*170G>A
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