Canonical Allele Identifier: CA476868973
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116832869-A-G
COSMIC: COSM4662528
MyVariant Identifiers: chr11:g.116703585A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832869A>G , CM000673.2:g.116832869A>G GRCh38
NC_000011.9:g.116703585A>G , CM000673.1:g.116703585A>G GRCh37
NC_000011.8:g.116208795A>G NCBI36
NG_008949.1:g.7962A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.285A>G MANE Select ENSP00000227667.2:p.Ser95=
ENST00000227667.7:c.285A>G ENSP00000227667.2:p.Ser95=
ENST00000375345.3:c.339A>G ENSP00000364494.1:p.Ser113=
ENST00000630701.1:c.339A>G ENSP00000486182.1:p.Ser113=
NM_000040.1:c.285A>G NP_000031.1:p.Ser95=
NM_000040.2:c.285A>G NP_000031.1:p.Ser95=
NM_000040.3:c.285A>G MANE Select NP_000031.1:p.Ser95=
Search 100 bp 5'
Search 100 bp 3'