Canonical Allele Identifier: CA2002758870
Gene: APOC3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830723G= , CM000673.2:g.116830723G= GRCh38
NC_000011.9:g.116701439G= , CM000673.1:g.116701439G= GRCh37
NC_000011.8:g.116206649G= NCBI36
NG_008949.1:g.5816G=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-50G= MANE Select ENSP00000227667.2:n.56-50G=
ENST00000227667.7:c.56-50G= ENSP00000227667.2:n.56-50G=
ENST00000375345.3:c.110-50G= ENSP00000364494.1:n.110-50G=
ENST00000433777.5:c.56-50G= ENSP00000410614.1:n.56-50G=
ENST00000470144.1:n.88-50G=
ENST00000630701.1:c.110-50G= ENSP00000486182.1:n.110-50G=
NM_000040.1:c.56-50G= NP_000031.1:n.56-50G=
NM_000040.2:c.56-50G= NP_000031.1:n.56-50G=
NM_000040.3:c.56-50G= MANE Select NP_000031.1:n.56-50G=
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