Canonical Allele Identifier: CA2002760351
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832932T= , CM000673.2:g.116832932T= GRCh38
NC_000011.9:g.116703648T= , CM000673.1:g.116703648T= GRCh37
NC_000011.8:g.116208858T= NCBI36
NG_008949.1:g.8025T=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*48T= MANE Select ENSP00000227667.2:n.*48T=
ENST00000227667.7:c.*48T= ENSP00000227667.2:n.*48T=
ENST00000375345.3:c.*48T= ENSP00000364494.1:n.*48T=
ENST00000630701.1:c.402T= ENSP00000486182.1:n.402T=
NM_000040.1:c.*48T= NP_000031.1:n.*48T=
NM_000040.2:c.*48T= NP_000031.1:n.*48T=
NM_000040.3:c.*48T= MANE Select NP_000031.1:n.*48T=