Canonical Allele Identifier: CA476868962
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116832857-C-A
MyVariant Identifiers: chr11:g.116703573C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832857C>A , CM000673.2:g.116832857C>A GRCh38
NC_000011.9:g.116703573C>A , CM000673.1:g.116703573C>A GRCh37
NC_000011.8:g.116208783C>A NCBI36
NG_008949.1:g.7950C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.273C>A MANE Select ENSP00000227667.2:p.Val91=
ENST00000227667.7:c.273C>A ENSP00000227667.2:p.Val91=
ENST00000375345.3:c.327C>A ENSP00000364494.1:p.Val109=
ENST00000630701.1:c.327C>A ENSP00000486182.1:p.Val109=
NM_000040.1:c.273C>A NP_000031.1:p.Val91=
NM_000040.2:c.273C>A NP_000031.1:p.Val91=
NM_000040.3:c.273C>A MANE Select NP_000031.1:p.Val91=
Search 100 bp 5'
Search 100 bp 3'