Canonical Allele Identifier: CA2616111411
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833052-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833052C>T , CM000673.2:g.116833052C>T GRCh38
NC_000011.9:g.116703768C>T , CM000673.1:g.116703768C>T GRCh37
NC_000011.8:g.116208978C>T NCBI36
NG_008949.1:g.8145C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*168C>T MANE Select ENSP00000227667.2:n.*168C>T
ENST00000227667.7:c.*168C>T ENSP00000227667.2:n.*168C>T
ENST00000375345.3:c.*168C>T ENSP00000364494.1:n.*168C>T
ENST00000630701.1:c.522C>T ENSP00000486182.1:n.522C>T
NM_000040.1:c.*168C>T NP_000031.1:n.*168C>T
NM_000040.2:c.*168C>T NP_000031.1:n.*168C>T
NM_000040.3:c.*168C>T MANE Select NP_000031.1:n.*168C>T
Search 100 bp 5'
Search 100 bp 3'