Canonical Allele Identifier: CA2002760356
Gene: APOC3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832942A= , CM000673.2:g.116832942A= GRCh38
NC_000011.9:g.116703658A= , CM000673.1:g.116703658A= GRCh37
NC_000011.8:g.116208868A= NCBI36
NG_008949.1:g.8035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*58A= MANE Select ENSP00000227667.2:n.*58A=
ENST00000227667.7:c.*58A= ENSP00000227667.2:n.*58A=
ENST00000375345.3:c.*58A= ENSP00000364494.1:n.*58A=
ENST00000630701.1:c.412A= ENSP00000486182.1:n.412A=
NM_000040.1:c.*58A= NP_000031.1:n.*58A=
NM_000040.2:c.*58A= NP_000031.1:n.*58A=
NM_000040.3:c.*58A= MANE Select NP_000031.1:n.*58A=
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