Canonical Allele Identifier: CA2493473145
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002787G= , CM000664.2:g.21002787G= GRCh38
NC_000002.11:g.21225659G= , CM000664.1:g.21225659G= GRCh37
NC_000002.10:g.21079164G= NCBI36
NG_011793.1:g.46287C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12635C= MANE Select ENSP00000233242.1:p.Thr4212=
ENST00000616098.4:c.12635C= ENSP00000477990.1:p.Thr4212=
NM_000384.2:c.12635C= NP_000375.2:p.Thr4212=
XM_011532809.1:c.5870-3514C= XP_011531111.1:n.5870-3514C=
NM_000384.3:c.12635C= MANE Select NP_000375.3:p.Thr4212=
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