Canonical Allele Identifier: CA2493476564
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010143C= , CM000664.2:g.21010143C= GRCh38
NC_000002.11:g.21233015C= , CM000664.1:g.21233015C= GRCh37
NC_000002.10:g.21086520C= NCBI36
NG_011793.1:g.38931G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6725G= MANE Select ENSP00000233242.1:p.Gly2242=
ENST00000616098.4:c.6725G= ENSP00000477990.1:p.Gly2242=
NM_000384.2:c.6725G= NP_000375.2:p.Gly2242=
XM_011532809.1:c.5869+590G= XP_011531111.1:n.5869+590G=
NM_000384.3:c.6725G= MANE Select NP_000375.3:p.Gly2242=