Canonical Allele Identifier: CA2493476956
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011012A= , CM000664.2:g.21011012A= GRCh38
NC_000002.11:g.21233884A= , CM000664.1:g.21233884A= GRCh37
NC_000002.10:g.21087389A= NCBI36
NG_011793.1:g.38062T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5856T= MANE Select ENSP00000233242.1:p.His1952=
ENST00000616098.4:c.5856T= ENSP00000477990.1:p.His1952=
NM_000384.2:c.5856T= NP_000375.2:p.His1952=
XM_011532809.1:c.5856T= XP_011531111.1:p.His1952=
NM_000384.3:c.5856T= MANE Select NP_000375.3:p.His1952=
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