Canonical Allele Identifier: CA2493475066
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007000C= , CM000664.2:g.21007000C= GRCh38
NC_000002.11:g.21229872C= , CM000664.1:g.21229872C= GRCh37
NC_000002.10:g.21083377C= NCBI36
NG_011793.1:g.42074G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9868G= MANE Select ENSP00000233242.1:p.Val3290=
ENST00000616098.4:c.9868G= ENSP00000477990.1:p.Val3290=
NM_000384.2:c.9868G= NP_000375.2:p.Val3290=
XM_011532809.1:c.5869+3733G= XP_011531111.1:n.5869+3733G=
NM_000384.3:c.9868G= MANE Select NP_000375.3:p.Val3290=