Canonical Allele Identifier: CA6289711
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs748747574
ExAC: 11:116703610 A / C
gnomAD v2: 11-116703610-A-C
gnomAD v4: 11-116832894-A-C
MyVariant Identifiers: chr11:g.116703610A>C (hg19) chr11:g.116832894A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832894A>C , CM000673.2:g.116832894A>C GRCh38
NC_000011.9:g.116703610A>C , CM000673.1:g.116703610A>C GRCh37
NC_000011.8:g.116208820A>C NCBI36
NG_008949.1:g.7987A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*10A>C MANE Select ENSP00000227667.2:n.*10A>C
ENST00000227667.7:c.*10A>C ENSP00000227667.2:n.*10A>C
ENST00000375345.3:c.*10A>C ENSP00000364494.1:n.*10A>C
ENST00000630701.1:c.364A>C ENSP00000486182.1:n.364A>C
NM_000040.1:c.*10A>C NP_000031.1:n.*10A>C
NM_000040.2:c.*10A>C NP_000031.1:n.*10A>C
NM_000040.3:c.*10A>C MANE Select NP_000031.1:n.*10A>C
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