Canonical Allele Identifier: CA2493472675
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001902G= , CM000664.2:g.21001902G= GRCh38
NC_000002.11:g.21224774G= , CM000664.1:g.21224774G= GRCh37
NC_000002.10:g.21078279G= NCBI36
NG_011793.1:g.47172C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13520C= MANE Select ENSP00000233242.1:p.Ser4507=
ENST00000616098.4:c.13518C= ENSP00000477990.1:n.13518C=
NM_000384.2:c.13520C= NP_000375.2:p.Ser4507=
XM_011532809.1:c.5870-2629C= XP_011531111.1:n.5870-2629C=
NM_000384.3:c.13520C= MANE Select NP_000375.3:p.Ser4507=