Canonical Allele Identifier: CA382711300
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832811C>A , CM000673.2:g.116832811C>A GRCh38
NC_000011.9:g.116703527C>A , CM000673.1:g.116703527C>A GRCh37
NC_000011.8:g.116208737C>A NCBI36
NG_008949.1:g.7904C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.227C>A MANE Select ENSP00000227667.2:p.Thr76Asn
ENST00000227667.7:c.227C>A ENSP00000227667.2:p.Thr76Asn
ENST00000375345.3:c.281C>A ENSP00000364494.1:p.Thr94Asn
ENST00000630701.1:c.281C>A ENSP00000486182.1:p.Thr94Asn
NM_000040.1:c.227C>A NP_000031.1:p.Thr76Asn
NM_000040.2:c.227C>A NP_000031.1:p.Thr76Asn
NM_000040.3:c.227C>A MANE Select NP_000031.1:p.Thr76Asn