Canonical Allele Identifier: CA2616111348
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116832991-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832991G>T , CM000673.2:g.116832991G>T GRCh38
NC_000011.9:g.116703707G>T , CM000673.1:g.116703707G>T GRCh37
NC_000011.8:g.116208917G>T NCBI36
NG_008949.1:g.8084G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*107G>T MANE Select ENSP00000227667.2:n.*107G>T
ENST00000227667.7:c.*107G>T ENSP00000227667.2:n.*107G>T
ENST00000375345.3:c.*107G>T ENSP00000364494.1:n.*107G>T
ENST00000630701.1:c.461G>T ENSP00000486182.1:n.461G>T
NM_000040.1:c.*107G>T NP_000031.1:n.*107G>T
NM_000040.2:c.*107G>T NP_000031.1:n.*107G>T
NM_000040.3:c.*107G>T MANE Select NP_000031.1:n.*107G>T
Search 100 bp 5'
Search 100 bp 3'