Canonical Allele Identifier: CA2616111378
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833021-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833021C>G , CM000673.2:g.116833021C>G GRCh38
NC_000011.9:g.116703737C>G , CM000673.1:g.116703737C>G GRCh37
NC_000011.8:g.116208947C>G NCBI36
NG_008949.1:g.8114C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*137C>G MANE Select ENSP00000227667.2:n.*137C>G
ENST00000227667.7:c.*137C>G ENSP00000227667.2:n.*137C>G
ENST00000375345.3:c.*137C>G ENSP00000364494.1:n.*137C>G
ENST00000630701.1:c.491C>G ENSP00000486182.1:n.491C>G
NM_000040.1:c.*137C>G NP_000031.1:n.*137C>G
NM_000040.2:c.*137C>G NP_000031.1:n.*137C>G
NM_000040.3:c.*137C>G MANE Select NP_000031.1:n.*137C>G
Search 100 bp 5'
Search 100 bp 3'