Canonical Allele Identifier: CA2616110945
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830735A>G , CM000673.2:g.116830735A>G GRCh38
NC_000011.9:g.116701451A>G , CM000673.1:g.116701451A>G GRCh37
NC_000011.8:g.116206661A>G NCBI36
NG_008949.1:g.5828A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-38A>G MANE Select ENSP00000227667.2:n.56-38A>G
ENST00000227667.7:c.56-38A>G ENSP00000227667.2:n.56-38A>G
ENST00000375345.3:c.110-38A>G ENSP00000364494.1:n.110-38A>G
ENST00000433777.5:c.56-38A>G ENSP00000410614.1:n.56-38A>G
ENST00000470144.1:n.88-38A>G
ENST00000630701.1:c.110-38A>G ENSP00000486182.1:n.110-38A>G
NM_000040.1:c.56-38A>G NP_000031.1:n.56-38A>G
NM_000040.2:c.56-38A>G NP_000031.1:n.56-38A>G
NM_000040.3:c.56-38A>G MANE Select NP_000031.1:n.56-38A>G