Canonical Allele Identifier: CA2616111367
Gene: APOC3 HGNC NCBI

Linked Data

gnomAD v4: 11-116833012-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833012T>C , CM000673.2:g.116833012T>C GRCh38
NC_000011.9:g.116703728T>C , CM000673.1:g.116703728T>C GRCh37
NC_000011.8:g.116208938T>C NCBI36
NG_008949.1:g.8105T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*128T>C MANE Select ENSP00000227667.2:n.*128T>C
ENST00000227667.7:c.*128T>C ENSP00000227667.2:n.*128T>C
ENST00000375345.3:c.*128T>C ENSP00000364494.1:n.*128T>C
ENST00000630701.1:c.482T>C ENSP00000486182.1:n.482T>C
NM_000040.1:c.*128T>C NP_000031.1:n.*128T>C
NM_000040.2:c.*128T>C NP_000031.1:n.*128T>C
NM_000040.3:c.*128T>C MANE Select NP_000031.1:n.*128T>C
Search 100 bp 5'
Search 100 bp 3'