Canonical Allele Identifier: CA2493476929
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010983G= , CM000664.2:g.21010983G= GRCh38
NC_000002.11:g.21233855G= , CM000664.1:g.21233855G= GRCh37
NC_000002.10:g.21087360G= NCBI36
NG_011793.1:g.38091C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5885C= MANE Select ENSP00000233242.1:p.Ala1962=
ENST00000616098.4:c.5885C= ENSP00000477990.1:p.Ala1962=
NM_000384.2:c.5885C= NP_000375.2:p.Ala1962=
XM_011532809.1:c.5864+21C= XP_011531111.1:n.5864+21C=
NM_000384.3:c.5885C= MANE Select NP_000375.3:p.Ala1962=