Canonical Allele Identifier: CA382710010
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830826A>T , CM000673.2:g.116830826A>T GRCh38
NC_000011.9:g.116701542A>T , CM000673.1:g.116701542A>T GRCh37
NC_000011.8:g.116206752A>T NCBI36
NG_008949.1:g.5919A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.109A>T MANE Select ENSP00000227667.2:p.Lys37Ter
ENST00000227667.7:c.109A>T ENSP00000227667.2:p.Lys37Ter
ENST00000375345.3:c.163A>T ENSP00000364494.1:p.Lys55Ter
ENST00000433777.5:c.109A>T ENSP00000410614.1:p.Lys37Ter
ENST00000470144.1:n.141A>T
ENST00000630701.1:c.163A>T ENSP00000486182.1:p.Lys55Ter
NM_000040.1:c.109A>T NP_000031.1:p.Lys37Ter
NM_000040.2:c.109A>T NP_000031.1:p.Lys37Ter
NM_000040.3:c.109A>T MANE Select NP_000031.1:p.Lys37Ter