Canonical Allele Identifier: CA382711579
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703566C>G (hg19) chr11:g.116832850C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832850C>G , CM000673.2:g.116832850C>G GRCh38
NC_000011.9:g.116703566C>G , CM000673.1:g.116703566C>G GRCh37
NC_000011.8:g.116208776C>G NCBI36
NG_008949.1:g.7943C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.266C>G MANE Select ENSP00000227667.2:p.Pro89Arg
ENST00000227667.7:c.266C>G ENSP00000227667.2:p.Pro89Arg
ENST00000375345.3:c.320C>G ENSP00000364494.1:p.Pro107Arg
ENST00000630701.1:c.320C>G ENSP00000486182.1:p.Pro107Arg
NM_000040.1:c.266C>G NP_000031.1:p.Pro89Arg
NM_000040.2:c.266C>G NP_000031.1:p.Pro89Arg
NM_000040.3:c.266C>G MANE Select NP_000031.1:p.Pro89Arg
Search 100 bp 5'
Search 100 bp 3'