Canonical Allele Identifier: CA2493476311
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009611G= , CM000664.2:g.21009611G= GRCh38
NC_000002.11:g.21232483G= , CM000664.1:g.21232483G= GRCh37
NC_000002.10:g.21085988G= NCBI36
NG_011793.1:g.39463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7257C= MANE Select ENSP00000233242.1:p.Phe2419=
ENST00000616098.4:c.7257C= ENSP00000477990.1:p.Phe2419=
NM_000384.2:c.7257C= NP_000375.2:p.Phe2419=
XM_011532809.1:c.5869+1122C= XP_011531111.1:n.5869+1122C=
NM_000384.3:c.7257C= MANE Select NP_000375.3:p.Phe2419=
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