Canonical Allele Identifier: CA6289719
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs769165532

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832930C>A , CM000673.2:g.116832930C>A GRCh38
NC_000011.9:g.116703646C>A , CM000673.1:g.116703646C>A GRCh37
NC_000011.8:g.116208856C>A NCBI36
NG_008949.1:g.8023C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*46C>A MANE Select ENSP00000227667.2:n.*46C>A
ENST00000227667.7:c.*46C>A ENSP00000227667.2:n.*46C>A
ENST00000375345.3:c.*46C>A ENSP00000364494.1:n.*46C>A
ENST00000630701.1:c.400C>A ENSP00000486182.1:n.400C>A
NM_000040.1:c.*46C>A NP_000031.1:n.*46C>A
NM_000040.2:c.*46C>A NP_000031.1:n.*46C>A
NM_000040.3:c.*46C>A MANE Select NP_000031.1:n.*46C>A