Canonical Allele Identifier: CA476868971

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703582T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832866T>G , CM000673.2:g.116832866T>G	GRCh38
NC_000011.9:g.116703582T>G , CM000673.1:g.116703582T>G	GRCh37
NC_000011.8:g.116208792T>G	NCBI36
NG_008949.1:g.7959T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.282T>G MANE Select	ENSP00000227667.2:p.Thr94=
ENST00000227667.7:c.282T>G	ENSP00000227667.2:p.Thr94=
ENST00000375345.3:c.336T>G	ENSP00000364494.1:p.Thr112=
ENST00000630701.1:c.336T>G	ENSP00000486182.1:p.Thr112=
NM_000040.1:c.282T>G	NP_000031.1:p.Thr94=
NM_000040.2:c.282T>G	NP_000031.1:p.Thr94=
NM_000040.3:c.282T>G MANE Select	NP_000031.1:p.Thr94=