Canonical Allele Identifier: CA477048372

Gene: APOC3

Linked Data

• gnomAD v4: 11-116830636-C-T
• MyVariant Identifiers: chr11:g.116701352C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830636C>T , CM000673.2:g.116830636C>T	GRCh38
NC_000011.9:g.116701352C>T , CM000673.1:g.116701352C>T	GRCh37
NC_000011.8:g.116206562C>T	NCBI36
NG_008949.1:g.5729C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.54C>T MANE Select	ENSP00000227667.2:p.Ala18=
ENST00000227667.7:c.54C>T	ENSP00000227667.2:p.Ala18=
ENST00000375345.3:c.108C>T	ENSP00000364494.1:p.Ala36=
ENST00000433777.5:c.54C>T	ENSP00000410614.1:p.Ala18=
ENST00000470144.1:n.86C>T
ENST00000630701.1:c.108C>T	ENSP00000486182.1:p.Ala36=
NM_000040.1:c.54C>T	NP_000031.1:p.Ala18=
NM_000040.2:c.54C>T	NP_000031.1:p.Ala18=
NM_000040.3:c.54C>T MANE Select	NP_000031.1:p.Ala18=