Canonical Allele Identifier: CA2493476729
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010512G= , CM000664.2:g.21010512G= GRCh38
NC_000002.11:g.21233384G= , CM000664.1:g.21233384G= GRCh37
NC_000002.10:g.21086889G= NCBI36
NG_011793.1:g.38562C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6356C= MANE Select ENSP00000233242.1:p.Pro2119=
ENST00000616098.4:c.6356C= ENSP00000477990.1:p.Pro2119=
NM_000384.2:c.6356C= NP_000375.2:p.Pro2119=
XM_011532809.1:c.5869+221C= XP_011531111.1:n.5869+221C=
NM_000384.3:c.6356C= MANE Select NP_000375.3:p.Pro2119=
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