Canonical Allele Identifier: CA476868987
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1306748259

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832978G>T , CM000673.2:g.116832978G>T GRCh38
NC_000011.9:g.116703694G>T , CM000673.1:g.116703694G>T GRCh37
NC_000011.8:g.116208904G>T NCBI36
NG_008949.1:g.8071G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*94G>T MANE Select ENSP00000227667.2:n.*94G>T
ENST00000227667.7:c.*94G>T ENSP00000227667.2:n.*94G>T
ENST00000375345.3:c.*94G>T ENSP00000364494.1:n.*94G>T
ENST00000630701.1:c.448G>T ENSP00000486182.1:n.448G>T
NM_000040.1:c.*94G>T NP_000031.1:n.*94G>T
NM_000040.2:c.*94G>T NP_000031.1:n.*94G>T
NM_000040.3:c.*94G>T MANE Select NP_000031.1:n.*94G>T