Canonical Allele Identifier: CA382709639
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116701335G>C (hg19) chr11:g.116830619G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830619G>C , CM000673.2:g.116830619G>C GRCh38
NC_000011.9:g.116701335G>C , CM000673.1:g.116701335G>C GRCh37
NC_000011.8:g.116206545G>C NCBI36
NG_008949.1:g.5712G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.37G>C MANE Select ENSP00000227667.2:p.Ala13Pro
ENST00000227667.7:c.37G>C ENSP00000227667.2:p.Ala13Pro
ENST00000375345.3:c.91G>C ENSP00000364494.1:p.Ala31Pro
ENST00000433777.5:c.37G>C ENSP00000410614.1:p.Ala13Pro
ENST00000470144.1:n.69G>C
ENST00000630701.1:c.91G>C ENSP00000486182.1:p.Ala31Pro
NM_000040.1:c.37G>C NP_000031.1:p.Ala13Pro
NM_000040.2:c.37G>C NP_000031.1:p.Ala13Pro
NM_000040.3:c.37G>C MANE Select NP_000031.1:p.Ala13Pro
Search 100 bp 5'
Search 100 bp 3'