Canonical Allele Identifier: CA2493476807
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010702C= , CM000664.2:g.21010702C= GRCh38
NC_000002.11:g.21233574C= , CM000664.1:g.21233574C= GRCh37
NC_000002.10:g.21087079C= NCBI36
NG_011793.1:g.38372G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6166G= MANE Select ENSP00000233242.1:p.Ala2056=
ENST00000616098.4:c.6166G= ENSP00000477990.1:p.Ala2056=
NM_000384.2:c.6166G= NP_000375.2:p.Ala2056=
XM_011532809.1:c.5869+31G= XP_011531111.1:n.5869+31G=
NM_000384.3:c.6166G= MANE Select NP_000375.3:p.Ala2056=
Search 100 bp 5'
Search 100 bp 3'