Canonical Allele Identifier: CA382711556
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703562G>C (hg19) chr11:g.116832846G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832846G>C , CM000673.2:g.116832846G>C GRCh38
NC_000011.9:g.116703562G>C , CM000673.1:g.116703562G>C GRCh37
NC_000011.8:g.116208772G>C NCBI36
NG_008949.1:g.7939G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.262G>C MANE Select ENSP00000227667.2:p.Asp88His
ENST00000227667.7:c.262G>C ENSP00000227667.2:p.Asp88His
ENST00000375345.3:c.316G>C ENSP00000364494.1:p.Asp106His
ENST00000630701.1:c.316G>C ENSP00000486182.1:p.Asp106His
NM_000040.1:c.262G>C NP_000031.1:p.Asp88His
NM_000040.2:c.262G>C NP_000031.1:p.Asp88His
NM_000040.3:c.262G>C MANE Select NP_000031.1:p.Asp88His
Search 100 bp 5'
Search 100 bp 3'