Canonical Allele Identifier: CA382711126

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703494A>T (hg19) ; chr11:g.116832778A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832778A>T , CM000673.2:g.116832778A>T	GRCh38
NC_000011.9:g.116703494A>T , CM000673.1:g.116703494A>T	GRCh37
NC_000011.8:g.116208704A>T	NCBI36
NG_008949.1:g.7871A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.194A>T MANE Select	ENSP00000227667.2:p.Asp65Val
ENST00000227667.7:c.194A>T	ENSP00000227667.2:p.Asp65Val
ENST00000375345.3:c.248A>T	ENSP00000364494.1:p.Asp83Val
ENST00000630701.1:c.248A>T	ENSP00000486182.1:p.Asp83Val
NM_000040.1:c.194A>T	NP_000031.1:p.Asp65Val
NM_000040.2:c.194A>T	NP_000031.1:p.Asp65Val
NM_000040.3:c.194A>T MANE Select	NP_000031.1:p.Asp65Val