Canonical Allele Identifier: CA2493472658
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001869T= , CM000664.2:g.21001869T= GRCh38
NC_000002.11:g.21224741T= , CM000664.1:g.21224741T= GRCh37
NC_000002.10:g.21078246T= NCBI36
NG_011793.1:g.47205A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13553A= MANE Select ENSP00000233242.1:p.Lys4518=
ENST00000616098.4:c.13551A= ENSP00000477990.1:n.13551A=
NM_000384.2:c.13553A= NP_000375.2:p.Lys4518=
XM_011532809.1:c.5870-2596A= XP_011531111.1:n.5870-2596A=
NM_000384.3:c.13553A= MANE Select NP_000375.3:p.Lys4518=