Canonical Allele Identifier: CA2493472867
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002220T= , CM000664.2:g.21002220T= GRCh38
NC_000002.11:g.21225092T= , CM000664.1:g.21225092T= GRCh37
NC_000002.10:g.21078597T= NCBI36
NG_011793.1:g.46854A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13202A= MANE Select ENSP00000233242.1:p.Tyr4401=
ENST00000616098.4:c.13200A= ENSP00000477990.1:n.13200A=
NM_000384.2:c.13202A= NP_000375.2:p.Tyr4401=
XM_011532809.1:c.5870-2947A= XP_011531111.1:n.5870-2947A=
NM_000384.3:c.13202A= MANE Select NP_000375.3:p.Tyr4401=