Canonical Allele Identifier: CA382711406
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832826T>A , CM000673.2:g.116832826T>A GRCh38
NC_000011.9:g.116703542T>A , CM000673.1:g.116703542T>A GRCh37
NC_000011.8:g.116208752T>A NCBI36
NG_008949.1:g.7919T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.242T>A MANE Select ENSP00000227667.2:p.Phe81Tyr
ENST00000227667.7:c.242T>A ENSP00000227667.2:p.Phe81Tyr
ENST00000375345.3:c.296T>A ENSP00000364494.1:p.Phe99Tyr
ENST00000630701.1:c.296T>A ENSP00000486182.1:p.Phe99Tyr
NM_000040.1:c.242T>A NP_000031.1:p.Phe81Tyr
NM_000040.2:c.242T>A NP_000031.1:p.Phe81Tyr
NM_000040.3:c.242T>A MANE Select NP_000031.1:p.Phe81Tyr