Canonical Allele Identifier: CA2493475091
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007057C= , CM000664.2:g.21007057C= GRCh38
NC_000002.11:g.21229929C= , CM000664.1:g.21229929C= GRCh37
NC_000002.10:g.21083434C= NCBI36
NG_011793.1:g.42017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9811G= MANE Select ENSP00000233242.1:p.Gly3271=
ENST00000616098.4:c.9811G= ENSP00000477990.1:p.Gly3271=
NM_000384.2:c.9811G= NP_000375.2:p.Gly3271=
XM_011532809.1:c.5869+3676G= XP_011531111.1:n.5869+3676G=
NM_000384.3:c.9811G= MANE Select NP_000375.3:p.Gly3271=
Search 100 bp 5'
Search 100 bp 3'