Canonical Allele Identifier: CA2493472579
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001714G= , CM000664.2:g.21001714G= GRCh38
NC_000002.11:g.21224586G= , CM000664.1:g.21224586G= GRCh37
NC_000002.10:g.21078091G= NCBI36
NG_011793.1:g.47360C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*16C= MANE Select ENSP00000233242.1:n.*16C=
ENST00000616098.4:c.13706C= ENSP00000477990.1:n.13706C=
NM_000384.2:c.*16C= NP_000375.2:n.*16C=
XM_011532809.1:c.5870-2441C= XP_011531111.1:n.5870-2441C=
NM_000384.3:c.*16C= MANE Select NP_000375.3:n.*16C=