Canonical Allele Identifier: CA2493472576
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001712A= , CM000664.2:g.21001712A= GRCh38
NC_000002.11:g.21224584A= , CM000664.1:g.21224584A= GRCh37
NC_000002.10:g.21078089A= NCBI36
NG_011793.1:g.47362T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*18T= MANE Select ENSP00000233242.1:n.*18T=
ENST00000616098.4:c.13708T= ENSP00000477990.1:n.13708T=
NM_000384.2:c.*18T= NP_000375.2:n.*18T=
XM_011532809.1:c.5870-2439T= XP_011531111.1:n.5870-2439T=
NM_000384.3:c.*18T= MANE Select NP_000375.3:n.*18T=