Canonical Allele Identifier: CA2493472559
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001665T= , CM000664.2:g.21001665T= GRCh38
NC_000002.11:g.21224537T= , CM000664.1:g.21224537T= GRCh37
NC_000002.10:g.21078042T= NCBI36
NG_011793.1:g.47409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*65A= MANE Select ENSP00000233242.1:n.*65A=
ENST00000616098.4:c.13755A= ENSP00000477990.1:n.13755A=
NM_000384.2:c.*65A= NP_000375.2:n.*65A=
XM_011532809.1:c.5870-2392A= XP_011531111.1:n.5870-2392A=
NM_000384.3:c.*65A= MANE Select NP_000375.3:n.*65A=