Canonical Allele Identifier: CA2493476707
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010442C= , CM000664.2:g.21010442C= GRCh38
NC_000002.11:g.21233314C= , CM000664.1:g.21233314C= GRCh37
NC_000002.10:g.21086819C= NCBI36
NG_011793.1:g.38632G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6426G= MANE Select ENSP00000233242.1:p.Leu2142=
ENST00000616098.4:c.6426G= ENSP00000477990.1:p.Leu2142=
NM_000384.2:c.6426G= NP_000375.2:p.Leu2142=
XM_011532809.1:c.5869+291G= XP_011531111.1:n.5869+291G=
NM_000384.3:c.6426G= MANE Select NP_000375.3:p.Leu2142=