Canonical Allele Identifier: CA382709752
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830771A>T , CM000673.2:g.116830771A>T GRCh38
NC_000011.9:g.116701487A>T , CM000673.1:g.116701487A>T GRCh37
NC_000011.8:g.116206697A>T NCBI36
NG_008949.1:g.5864A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.56-2A>T MANE Select ENSP00000227667.2:n.56-2A>T
ENST00000227667.7:c.56-2A>T ENSP00000227667.2:n.56-2A>T
ENST00000375345.3:c.110-2A>T ENSP00000364494.1:n.110-2A>T
ENST00000433777.5:c.56-2A>T ENSP00000410614.1:n.56-2A>T
ENST00000470144.1:n.88-2A>T
ENST00000630701.1:c.110-2A>T ENSP00000486182.1:n.110-2A>T
NM_000040.1:c.56-2A>T NP_000031.1:n.56-2A>T
NM_000040.2:c.56-2A>T NP_000031.1:n.56-2A>T
NM_000040.3:c.56-2A>T MANE Select NP_000031.1:n.56-2A>T