Canonical Allele Identifier: CA476868977

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703591G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832875G>T , CM000673.2:g.116832875G>T	GRCh38
NC_000011.9:g.116703591G>T , CM000673.1:g.116703591G>T	GRCh37
NC_000011.8:g.116208801G>T	NCBI36
NG_008949.1:g.7968G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.291G>T MANE Select	ENSP00000227667.2:p.Val97=
ENST00000227667.7:c.291G>T	ENSP00000227667.2:p.Val97=
ENST00000375345.3:c.345G>T	ENSP00000364494.1:p.Val115=
ENST00000630701.1:c.345G>T	ENSP00000486182.1:p.Val115=
NM_000040.1:c.291G>T	NP_000031.1:p.Val97=
NM_000040.2:c.291G>T	NP_000031.1:p.Val97=
NM_000040.3:c.291G>T MANE Select	NP_000031.1:p.Val97=