Canonical Allele Identifier: CA382711559

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703562G>T (hg19) ; chr11:g.116832846G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832846G>T , CM000673.2:g.116832846G>T	GRCh38
NC_000011.9:g.116703562G>T , CM000673.1:g.116703562G>T	GRCh37
NC_000011.8:g.116208772G>T	NCBI36
NG_008949.1:g.7939G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.262G>T MANE Select	ENSP00000227667.2:p.Asp88Tyr
ENST00000227667.7:c.262G>T	ENSP00000227667.2:p.Asp88Tyr
ENST00000375345.3:c.316G>T	ENSP00000364494.1:p.Asp106Tyr
ENST00000630701.1:c.316G>T	ENSP00000486182.1:p.Asp106Tyr
NM_000040.1:c.262G>T	NP_000031.1:p.Asp88Tyr
NM_000040.2:c.262G>T	NP_000031.1:p.Asp88Tyr
NM_000040.3:c.262G>T MANE Select	NP_000031.1:p.Asp88Tyr