Canonical Allele Identifier: CA476868984
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703597C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832881C>A , CM000673.2:g.116832881C>A GRCh38
NC_000011.9:g.116703597C>A , CM000673.1:g.116703597C>A GRCh37
NC_000011.8:g.116208807C>A NCBI36
NG_008949.1:g.7974C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.297C>A MANE Select ENSP00000227667.2:p.Ala99=
ENST00000227667.7:c.297C>A ENSP00000227667.2:p.Ala99=
ENST00000375345.3:c.351C>A ENSP00000364494.1:p.Ala117=
ENST00000630701.1:c.351C>A ENSP00000486182.1:p.Ala117=
NM_000040.1:c.297C>A NP_000031.1:p.Ala99=
NM_000040.2:c.297C>A NP_000031.1:p.Ala99=
NM_000040.3:c.297C>A MANE Select NP_000031.1:p.Ala99=
Search 100 bp 5'
Search 100 bp 3'