Canonical Allele Identifier: CA2002760313

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832864A= , CM000673.2:g.116832864A=	GRCh38
NC_000011.9:g.116703580A= , CM000673.1:g.116703580A=	GRCh37
NC_000011.8:g.116208790A=	NCBI36
NG_008949.1:g.7957A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.280A= MANE Select	ENSP00000227667.2:p.Thr94=
ENST00000227667.7:c.280A=	ENSP00000227667.2:p.Thr94=
ENST00000375345.3:c.334A=	ENSP00000364494.1:p.Thr112=
ENST00000630701.1:c.334A=	ENSP00000486182.1:p.Thr112=
NM_000040.1:c.280A=	NP_000031.1:p.Thr94=
NM_000040.2:c.280A=	NP_000031.1:p.Thr94=
NM_000040.3:c.280A= MANE Select	NP_000031.1:p.Thr94=