Canonical Allele Identifier: CA2002760297

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832834T= , CM000673.2:g.116832834T=	GRCh38
NC_000011.9:g.116703550T= , CM000673.1:g.116703550T=	GRCh37
NC_000011.8:g.116208760T=	NCBI36
NG_008949.1:g.7927T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.250T= MANE Select	ENSP00000227667.2:p.Phe84=
ENST00000227667.7:c.250T=	ENSP00000227667.2:p.Phe84=
ENST00000375345.3:c.304T=	ENSP00000364494.1:p.Phe102=
ENST00000630701.1:c.304T=	ENSP00000486182.1:p.Phe102=
NM_000040.1:c.250T=	NP_000031.1:p.Phe84=
NM_000040.2:c.250T=	NP_000031.1:p.Phe84=
NM_000040.3:c.250T= MANE Select	NP_000031.1:p.Phe84=