Canonical Allele Identifier: CA476869022
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941480612
gnomAD v3: 11-116833072-A-G
gnomAD v4: 11-116833072-A-G
MyVariant Identifiers: chr11:g.116703788A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833072A>G , CM000673.2:g.116833072A>G GRCh38
NC_000011.9:g.116703788A>G , CM000673.1:g.116703788A>G GRCh37
NC_000011.8:g.116208998A>G NCBI36
NG_008949.1:g.8165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*188A>G MANE Select ENSP00000227667.2:n.*188A>G
ENST00000227667.7:c.*188A>G ENSP00000227667.2:n.*188A>G
ENST00000375345.3:c.*188A>G ENSP00000364494.1:n.*188A>G
NM_000040.2:c.*188A>G NP_000031.1:n.*188A>G
NM_000040.3:c.*188A>G MANE Select NP_000031.1:n.*188A>G
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