Canonical Allele Identifier: CA2493473152
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002808G= , CM000664.2:g.21002808G= GRCh38
NC_000002.11:g.21225680G= , CM000664.1:g.21225680G= GRCh37
NC_000002.10:g.21079185G= NCBI36
NG_011793.1:g.46266C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12614C= MANE Select ENSP00000233242.1:p.Pro4205=
ENST00000616098.4:c.12614C= ENSP00000477990.1:p.Pro4205=
NM_000384.2:c.12614C= NP_000375.2:p.Pro4205=
XM_011532809.1:c.5870-3535C= XP_011531111.1:n.5870-3535C=
NM_000384.3:c.12614C= MANE Select NP_000375.3:p.Pro4205=
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