Canonical Allele Identifier: CA2002760272

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832770G= , CM000673.2:g.116832770G=	GRCh38
NC_000011.9:g.116703486G= , CM000673.1:g.116703486G=	GRCh37
NC_000011.8:g.116208696G=	NCBI36
NG_008949.1:g.7863G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.186G= MANE Select	ENSP00000227667.2:p.Trp62=
ENST00000227667.7:c.186G=	ENSP00000227667.2:p.Trp62=
ENST00000375345.3:c.240G=	ENSP00000364494.1:p.Trp80=
ENST00000630701.1:c.240G=	ENSP00000486182.1:p.Trp80=
NM_000040.1:c.186G=	NP_000031.1:p.Trp62=
NM_000040.2:c.186G=	NP_000031.1:p.Trp62=
NM_000040.3:c.186G= MANE Select	NP_000031.1:p.Trp62=