Canonical Allele Identifier: CA2493473037
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002548T= , CM000664.2:g.21002548T= GRCh38
NC_000002.11:g.21225420T= , CM000664.1:g.21225420T= GRCh37
NC_000002.10:g.21078925T= NCBI36
NG_011793.1:g.46526A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12874A= MANE Select ENSP00000233242.1:p.Thr4292=
ENST00000616098.4:c.12874A= ENSP00000477990.1:p.Thr4292=
NM_000384.2:c.12874A= NP_000375.2:p.Thr4292=
XM_011532809.1:c.5870-3275A= XP_011531111.1:n.5870-3275A=
NM_000384.3:c.12874A= MANE Select NP_000375.3:p.Thr4292=