Canonical Allele Identifier: CA382711293

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703526A>G (hg19) ; chr11:g.116832810A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832810A>G , CM000673.2:g.116832810A>G	GRCh38
NC_000011.9:g.116703526A>G , CM000673.1:g.116703526A>G	GRCh37
NC_000011.8:g.116208736A>G	NCBI36
NG_008949.1:g.7903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.226A>G MANE Select	ENSP00000227667.2:p.Thr76Ala
ENST00000227667.7:c.226A>G	ENSP00000227667.2:p.Thr76Ala
ENST00000375345.3:c.280A>G	ENSP00000364494.1:p.Thr94Ala
ENST00000630701.1:c.280A>G	ENSP00000486182.1:p.Thr94Ala
NM_000040.1:c.226A>G	NP_000031.1:p.Thr76Ala
NM_000040.2:c.226A>G	NP_000031.1:p.Thr76Ala
NM_000040.3:c.226A>G MANE Select	NP_000031.1:p.Thr76Ala