Canonical Allele Identifier: CA382711080
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832766G>A , CM000673.2:g.116832766G>A GRCh38
NC_000011.9:g.116703482G>A , CM000673.1:g.116703482G>A GRCh37
NC_000011.8:g.116208692G>A NCBI36
NG_008949.1:g.7859G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.182G>A MANE Select ENSP00000227667.2:p.Gly61Asp
ENST00000227667.7:c.182G>A ENSP00000227667.2:p.Gly61Asp
ENST00000375345.3:c.236G>A ENSP00000364494.1:p.Gly79Asp
ENST00000630701.1:c.236G>A ENSP00000486182.1:p.Gly79Asp
NM_000040.1:c.182G>A NP_000031.1:p.Gly61Asp
NM_000040.2:c.182G>A NP_000031.1:p.Gly61Asp
NM_000040.3:c.182G>A MANE Select NP_000031.1:p.Gly61Asp