Canonical Allele Identifier: CA477048351

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116701331C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830615C>G , CM000673.2:g.116830615C>G	GRCh38
NC_000011.9:g.116701331C>G , CM000673.1:g.116701331C>G	GRCh37
NC_000011.8:g.116206541C>G	NCBI36
NG_008949.1:g.5708C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.33C>G MANE Select	ENSP00000227667.2:p.Leu11=
ENST00000227667.7:c.33C>G	ENSP00000227667.2:p.Leu11=
ENST00000375345.3:c.87C>G	ENSP00000364494.1:p.Leu29=
ENST00000433777.5:c.33C>G	ENSP00000410614.1:p.Leu11=
ENST00000470144.1:n.65C>G
ENST00000630701.1:c.87C>G	ENSP00000486182.1:p.Leu29=
NM_000040.1:c.33C>G	NP_000031.1:p.Leu11=
NM_000040.2:c.33C>G	NP_000031.1:p.Leu11=
NM_000040.3:c.33C>G MANE Select	NP_000031.1:p.Leu11=