Canonical Allele Identifier: CA382711449
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832832A>T , CM000673.2:g.116832832A>T GRCh38
NC_000011.9:g.116703548A>T , CM000673.1:g.116703548A>T GRCh37
NC_000011.8:g.116208758A>T NCBI36
NG_008949.1:g.7925A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.248A>T MANE Select ENSP00000227667.2:p.Glu83Val
ENST00000227667.7:c.248A>T ENSP00000227667.2:p.Glu83Val
ENST00000375345.3:c.302A>T ENSP00000364494.1:p.Glu101Val
ENST00000630701.1:c.302A>T ENSP00000486182.1:p.Glu101Val
NM_000040.1:c.248A>T NP_000031.1:p.Glu83Val
NM_000040.2:c.248A>T NP_000031.1:p.Glu83Val
NM_000040.3:c.248A>T MANE Select NP_000031.1:p.Glu83Val