Canonical Allele Identifier: CA942608823
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941479334

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832959del , CM000673.2:g.116832959del GRCh38
NC_000011.9:g.116703675del , CM000673.1:g.116703675del GRCh37
NC_000011.8:g.116208885del NCBI36
NG_008949.1:g.8052del

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*75del MANE Select ENSP00000227667.2:n.*75del
ENST00000227667.7:c.*75del ENSP00000227667.2:n.*75del
ENST00000375345.3:c.*75del ENSP00000364494.1:n.*75del
ENST00000630701.1:c.429del ENSP00000486182.1:n.429del
NM_000040.1:c.*75del NP_000031.1:n.*75del
NM_000040.2:c.*75del NP_000031.1:n.*75del
NM_000040.3:c.*75del MANE Select NP_000031.1:n.*75del