Canonical Allele Identifier: CA2493472577
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001713A= , CM000664.2:g.21001713A= GRCh38
NC_000002.11:g.21224585A= , CM000664.1:g.21224585A= GRCh37
NC_000002.10:g.21078090A= NCBI36
NG_011793.1:g.47361T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*17T= MANE Select ENSP00000233242.1:n.*17T=
ENST00000616098.4:c.13707T= ENSP00000477990.1:n.13707T=
NM_000384.2:c.*17T= NP_000375.2:n.*17T=
XM_011532809.1:c.5870-2440T= XP_011531111.1:n.5870-2440T=
NM_000384.3:c.*17T= MANE Select NP_000375.3:n.*17T=