Canonical Allele Identifier: CA6289715
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs745586339
ExAC: 11:116703626 C / T
gnomAD v2: 11-116703626-C-T
gnomAD v3: 11-116832910-C-T
gnomAD v4: 11-116832910-C-T
MyVariant Identifiers: chr11:g.116703626C>T (hg19) chr11:g.116832910C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832910C>T , CM000673.2:g.116832910C>T GRCh38
NC_000011.9:g.116703626C>T , CM000673.1:g.116703626C>T GRCh37
NC_000011.8:g.116208836C>T NCBI36
NG_008949.1:g.8003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*26C>T MANE Select ENSP00000227667.2:n.*26C>T
ENST00000227667.7:c.*26C>T ENSP00000227667.2:n.*26C>T
ENST00000375345.3:c.*26C>T ENSP00000364494.1:n.*26C>T
ENST00000630701.1:c.380C>T ENSP00000486182.1:n.380C>T
NM_000040.1:c.*26C>T NP_000031.1:n.*26C>T
NM_000040.2:c.*26C>T NP_000031.1:n.*26C>T
NM_000040.3:c.*26C>T MANE Select NP_000031.1:n.*26C>T
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