Canonical Allele Identifier: CA477048215
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116701490A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830774A>G , CM000673.2:g.116830774A>G GRCh38
NC_000011.9:g.116701490A>G , CM000673.1:g.116701490A>G GRCh37
NC_000011.8:g.116206700A>G NCBI36
NG_008949.1:g.5867A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.57A>G MANE Select ENSP00000227667.2:p.Arg19=
ENST00000227667.7:c.57A>G ENSP00000227667.2:p.Arg19=
ENST00000375345.3:c.111A>G ENSP00000364494.1:p.Arg37=
ENST00000433777.5:c.57A>G ENSP00000410614.1:p.Arg19=
ENST00000470144.1:n.89A>G
ENST00000630701.1:c.111A>G ENSP00000486182.1:p.Arg37=
NM_000040.1:c.57A>G NP_000031.1:p.Arg19=
NM_000040.2:c.57A>G NP_000031.1:p.Arg19=
NM_000040.3:c.57A>G MANE Select NP_000031.1:p.Arg19=