Canonical Allele Identifier: CA2616111413
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833053-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833053T>C , CM000673.2:g.116833053T>C GRCh38
NC_000011.9:g.116703769T>C , CM000673.1:g.116703769T>C GRCh37
NC_000011.8:g.116208979T>C NCBI36
NG_008949.1:g.8146T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*169T>C MANE Select ENSP00000227667.2:n.*169T>C
ENST00000227667.7:c.*169T>C ENSP00000227667.2:n.*169T>C
ENST00000375345.3:c.*169T>C ENSP00000364494.1:n.*169T>C
ENST00000630701.1:c.523T>C ENSP00000486182.1:n.523T>C
NM_000040.1:c.*169T>C NP_000031.1:n.*169T>C
NM_000040.2:c.*169T>C NP_000031.1:n.*169T>C
NM_000040.3:c.*169T>C MANE Select NP_000031.1:n.*169T>C
Search 100 bp 5'
Search 100 bp 3'