Canonical Allele Identifier: CA6289613
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs747191960

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830612C>T , CM000673.2:g.116830612C>T GRCh38
NC_000011.9:g.116701328C>T , CM000673.1:g.116701328C>T GRCh37
NC_000011.8:g.116206538C>T NCBI36
NG_008949.1:g.5705C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.30C>T MANE Select ENSP00000227667.2:p.Ala10=
ENST00000227667.7:c.30C>T ENSP00000227667.2:p.Ala10=
ENST00000375345.3:c.84C>T ENSP00000364494.1:p.Ala28=
ENST00000433777.5:c.30C>T ENSP00000410614.1:p.Ala10=
ENST00000470144.1:n.62C>T
ENST00000630701.1:c.84C>T ENSP00000486182.1:p.Ala28=
NM_000040.1:c.30C>T NP_000031.1:p.Ala10=
NM_000040.2:c.30C>T NP_000031.1:p.Ala10=
NM_000040.3:c.30C>T MANE Select NP_000031.1:p.Ala10=