Canonical Allele Identifier: CA382711071
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832765G>C , CM000673.2:g.116832765G>C GRCh38
NC_000011.9:g.116703481G>C , CM000673.1:g.116703481G>C GRCh37
NC_000011.8:g.116208691G>C NCBI36
NG_008949.1:g.7858G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.181G>C MANE Select ENSP00000227667.2:p.Gly61Arg
ENST00000227667.7:c.181G>C ENSP00000227667.2:p.Gly61Arg
ENST00000375345.3:c.235G>C ENSP00000364494.1:p.Gly79Arg
ENST00000630701.1:c.235G>C ENSP00000486182.1:p.Gly79Arg
NM_000040.1:c.181G>C NP_000031.1:p.Gly61Arg
NM_000040.2:c.181G>C NP_000031.1:p.Gly61Arg
NM_000040.3:c.181G>C MANE Select NP_000031.1:p.Gly61Arg