Canonical Allele Identifier: CA382711120

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703491C>T (hg19) ; chr11:g.116832775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832775C>T , CM000673.2:g.116832775C>T	GRCh38
NC_000011.9:g.116703491C>T , CM000673.1:g.116703491C>T	GRCh37
NC_000011.8:g.116208701C>T	NCBI36
NG_008949.1:g.7868C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.191C>T MANE Select	ENSP00000227667.2:p.Thr64Ile
ENST00000227667.7:c.191C>T	ENSP00000227667.2:p.Thr64Ile
ENST00000375345.3:c.245C>T	ENSP00000364494.1:p.Thr82Ile
ENST00000630701.1:c.245C>T	ENSP00000486182.1:p.Thr82Ile
NM_000040.1:c.191C>T	NP_000031.1:p.Thr64Ile
NM_000040.2:c.191C>T	NP_000031.1:p.Thr64Ile
NM_000040.3:c.191C>T MANE Select	NP_000031.1:p.Thr64Ile