Canonical Allele Identifier: CA672202460
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1334964101
gnomAD v3: 11-116833065-T-C
gnomAD v4: 11-116833065-T-C
MyVariant Identifiers: chr11:g.116703781T>C (hg19) chr11:g.116833065T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833065T>C , CM000673.2:g.116833065T>C GRCh38
NC_000011.9:g.116703781T>C , CM000673.1:g.116703781T>C GRCh37
NC_000011.8:g.116208991T>C NCBI36
NG_008949.1:g.8158T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*181T>C MANE Select ENSP00000227667.2:n.*181T>C
ENST00000227667.7:c.*181T>C ENSP00000227667.2:n.*181T>C
ENST00000375345.3:c.*181T>C ENSP00000364494.1:n.*181T>C
ENST00000630701.1:c.535T>C ENSP00000486182.1:n.535T>C
NM_000040.1:c.*181T>C NP_000031.1:n.*181T>C
NM_000040.2:c.*181T>C NP_000031.1:n.*181T>C
NM_000040.3:c.*181T>C MANE Select NP_000031.1:n.*181T>C
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