Canonical Allele Identifier: CA2493476903
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010908A= , CM000664.2:g.21010908A= GRCh38
NC_000002.11:g.21233780A= , CM000664.1:g.21233780A= GRCh37
NC_000002.10:g.21087285A= NCBI36
NG_011793.1:g.38166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5960T= MANE Select ENSP00000233242.1:p.Phe1987=
ENST00000616098.4:c.5960T= ENSP00000477990.1:p.Phe1987=
NM_000384.2:c.5960T= NP_000375.2:p.Phe1987=
XM_011532809.1:c.5864+96T= XP_011531111.1:n.5864+96T=
NM_000384.3:c.5960T= MANE Select NP_000375.3:p.Phe1987=