Canonical Allele Identifier: CA2493472580
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001717T= , CM000664.2:g.21001717T= GRCh38
NC_000002.11:g.21224589T= , CM000664.1:g.21224589T= GRCh37
NC_000002.10:g.21078094T= NCBI36
NG_011793.1:g.47357A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*13A= MANE Select ENSP00000233242.1:n.*13A=
ENST00000616098.4:c.13703A= ENSP00000477990.1:n.13703A=
NM_000384.2:c.*13A= NP_000375.2:n.*13A=
XM_011532809.1:c.5870-2444A= XP_011531111.1:n.5870-2444A=
NM_000384.3:c.*13A= MANE Select NP_000375.3:n.*13A=