Canonical Allele Identifier: CA2616111368
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833015-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833015C>A , CM000673.2:g.116833015C>A GRCh38
NC_000011.9:g.116703731C>A , CM000673.1:g.116703731C>A GRCh37
NC_000011.8:g.116208941C>A NCBI36
NG_008949.1:g.8108C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*131C>A MANE Select ENSP00000227667.2:n.*131C>A
ENST00000227667.7:c.*131C>A ENSP00000227667.2:n.*131C>A
ENST00000375345.3:c.*131C>A ENSP00000364494.1:n.*131C>A
ENST00000630701.1:c.485C>A ENSP00000486182.1:n.485C>A
NM_000040.1:c.*131C>A NP_000031.1:n.*131C>A
NM_000040.2:c.*131C>A NP_000031.1:n.*131C>A
NM_000040.3:c.*131C>A MANE Select NP_000031.1:n.*131C>A
Search 100 bp 5'
Search 100 bp 3'