Canonical Allele Identifier: CA2002760301
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832842T= , CM000673.2:g.116832842T= GRCh38
NC_000011.9:g.116703558T= , CM000673.1:g.116703558T= GRCh37
NC_000011.8:g.116208768T= NCBI36
NG_008949.1:g.7935T=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.258T= MANE Select ENSP00000227667.2:p.Asp86=
ENST00000227667.7:c.258T= ENSP00000227667.2:p.Asp86=
ENST00000375345.3:c.312T= ENSP00000364494.1:p.Asp104=
ENST00000630701.1:c.312T= ENSP00000486182.1:p.Asp104=
NM_000040.1:c.258T= NP_000031.1:p.Asp86=
NM_000040.2:c.258T= NP_000031.1:p.Asp86=
NM_000040.3:c.258T= MANE Select NP_000031.1:p.Asp86=