Canonical Allele Identifier: CA2493476148
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009253C= , CM000664.2:g.21009253C= GRCh38
NC_000002.11:g.21232125C= , CM000664.1:g.21232125C= GRCh37
NC_000002.10:g.21085630C= NCBI36
NG_011793.1:g.39821G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7615G= MANE Select ENSP00000233242.1:p.Val2539=
ENST00000616098.4:c.7615G= ENSP00000477990.1:p.Val2539=
NM_000384.2:c.7615G= NP_000375.2:p.Val2539=
XM_011532809.1:c.5869+1480G= XP_011531111.1:n.5869+1480G=
NM_000384.3:c.7615G= MANE Select NP_000375.3:p.Val2539=
Search 100 bp 5'
Search 100 bp 3'