Canonical Allele Identifier: CA2493472859
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002202A= , CM000664.2:g.21002202A= GRCh38
NC_000002.11:g.21225074A= , CM000664.1:g.21225074A= GRCh37
NC_000002.10:g.21078579A= NCBI36
NG_011793.1:g.46872T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13220T= MANE Select ENSP00000233242.1:p.Ile4407=
ENST00000616098.4:c.13218T= ENSP00000477990.1:n.13218T=
NM_000384.2:c.13220T= NP_000375.2:p.Ile4407=
XM_011532809.1:c.5870-2929T= XP_011531111.1:n.5870-2929T=
NM_000384.3:c.13220T= MANE Select NP_000375.3:p.Ile4407=
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