Canonical Allele Identifier: CA2616111361
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833004-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833004C>G , CM000673.2:g.116833004C>G GRCh38
NC_000011.9:g.116703720C>G , CM000673.1:g.116703720C>G GRCh37
NC_000011.8:g.116208930C>G NCBI36
NG_008949.1:g.8097C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*120C>G MANE Select ENSP00000227667.2:n.*120C>G
ENST00000227667.7:c.*120C>G ENSP00000227667.2:n.*120C>G
ENST00000375345.3:c.*120C>G ENSP00000364494.1:n.*120C>G
ENST00000630701.1:c.474C>G ENSP00000486182.1:n.474C>G
NM_000040.1:c.*120C>G NP_000031.1:n.*120C>G
NM_000040.2:c.*120C>G NP_000031.1:n.*120C>G
NM_000040.3:c.*120C>G MANE Select NP_000031.1:n.*120C>G
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