Canonical Allele Identifier: CA229321222
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1032811450

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833002C>A , CM000673.2:g.116833002C>A GRCh38
NC_000011.9:g.116703718C>A , CM000673.1:g.116703718C>A GRCh37
NC_000011.8:g.116208928C>A NCBI36
NG_008949.1:g.8095C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*118C>A MANE Select ENSP00000227667.2:n.*118C>A
ENST00000227667.7:c.*118C>A ENSP00000227667.2:n.*118C>A
ENST00000375345.3:c.*118C>A ENSP00000364494.1:n.*118C>A
ENST00000630701.1:c.472C>A ENSP00000486182.1:n.472C>A
NM_000040.1:c.*118C>A NP_000031.1:n.*118C>A
NM_000040.2:c.*118C>A NP_000031.1:n.*118C>A
NM_000040.3:c.*118C>A MANE Select NP_000031.1:n.*118C>A