Canonical Allele Identifier: CA382709713

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116701355T>A (hg19) ; chr11:g.116830639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830639T>A , CM000673.2:g.116830639T>A	GRCh38
NC_000011.9:g.116701355T>A , CM000673.1:g.116701355T>A	GRCh37
NC_000011.8:g.116206565T>A	NCBI36
NG_008949.1:g.5732T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.55+2T>A MANE Select	ENSP00000227667.2:n.55+2T>A
ENST00000227667.7:c.55+2T>A	ENSP00000227667.2:n.55+2T>A
ENST00000375345.3:c.109+2T>A	ENSP00000364494.1:n.109+2T>A
ENST00000433777.5:c.55+2T>A	ENSP00000410614.1:n.55+2T>A
ENST00000470144.1:n.87+2T>A
ENST00000630701.1:c.109+2T>A	ENSP00000486182.1:n.109+2T>A
NM_000040.1:c.55+2T>A	NP_000031.1:n.55+2T>A
NM_000040.2:c.55+2T>A	NP_000031.1:n.55+2T>A
NM_000040.3:c.55+2T>A MANE Select	NP_000031.1:n.55+2T>A