Canonical Allele Identifier: CA2493477131
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011316T= , CM000664.2:g.21011316T= GRCh38
NC_000002.11:g.21234188T= , CM000664.1:g.21234188T= GRCh37
NC_000002.10:g.21087693T= NCBI36
NG_011793.1:g.37758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5552A= MANE Select ENSP00000233242.1:p.Tyr1851=
ENST00000616098.4:c.5552A= ENSP00000477990.1:p.Tyr1851=
NM_000384.2:c.5552A= NP_000375.2:p.Tyr1851=
XM_011532809.1:c.5552A= XP_011531111.1:p.Tyr1851=
NM_000384.3:c.5552A= MANE Select NP_000375.3:p.Tyr1851=
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