Canonical Allele Identifier: CA382711732

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703586G>T (hg19) ; chr11:g.116832870G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832870G>T , CM000673.2:g.116832870G>T	GRCh38
NC_000011.9:g.116703586G>T , CM000673.1:g.116703586G>T	GRCh37
NC_000011.8:g.116208796G>T	NCBI36
NG_008949.1:g.7963G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.286G>T MANE Select	ENSP00000227667.2:p.Ala96Ser
ENST00000227667.7:c.286G>T	ENSP00000227667.2:p.Ala96Ser
ENST00000375345.3:c.340G>T	ENSP00000364494.1:p.Ala114Ser
ENST00000630701.1:c.340G>T	ENSP00000486182.1:p.Ala114Ser
NM_000040.1:c.286G>T	NP_000031.1:p.Ala96Ser
NM_000040.2:c.286G>T	NP_000031.1:p.Ala96Ser
NM_000040.3:c.286G>T MANE Select	NP_000031.1:p.Ala96Ser