Canonical Allele Identifier: CA229321245
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1024296488
gnomAD v4: 11-116833035-C-T
MyVariant Identifiers: chr11:g.116833035C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833035C>T , CM000673.2:g.116833035C>T GRCh38
NC_000011.9:g.116703751C>T , CM000673.1:g.116703751C>T GRCh37
NC_000011.8:g.116208961C>T NCBI36
NG_008949.1:g.8128C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*151C>T MANE Select ENSP00000227667.2:n.*151C>T
ENST00000227667.7:c.*151C>T ENSP00000227667.2:n.*151C>T
ENST00000375345.3:c.*151C>T ENSP00000364494.1:n.*151C>T
ENST00000630701.1:c.505C>T ENSP00000486182.1:n.505C>T
NM_000040.1:c.*151C>T NP_000031.1:n.*151C>T
NM_000040.2:c.*151C>T NP_000031.1:n.*151C>T
NM_000040.3:c.*151C>T MANE Select NP_000031.1:n.*151C>T
Search 100 bp 5'
Search 100 bp 3'