Canonical Allele Identifier: CA382711788
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703590T>C (hg19) chr11:g.116832874T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832874T>C , CM000673.2:g.116832874T>C GRCh38
NC_000011.9:g.116703590T>C , CM000673.1:g.116703590T>C GRCh37
NC_000011.8:g.116208800T>C NCBI36
NG_008949.1:g.7967T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.290T>C MANE Select ENSP00000227667.2:p.Val97Ala
ENST00000227667.7:c.290T>C ENSP00000227667.2:p.Val97Ala
ENST00000375345.3:c.344T>C ENSP00000364494.1:p.Val115Ala
ENST00000630701.1:c.344T>C ENSP00000486182.1:p.Val115Ala
NM_000040.1:c.290T>C NP_000031.1:p.Val97Ala
NM_000040.2:c.290T>C NP_000031.1:p.Val97Ala
NM_000040.3:c.290T>C MANE Select NP_000031.1:p.Val97Ala
Search 100 bp 5'
Search 100 bp 3'