Canonical Allele Identifier: CA2493472569
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001692T= , CM000664.2:g.21001692T= GRCh38
NC_000002.11:g.21224564T= , CM000664.1:g.21224564T= GRCh37
NC_000002.10:g.21078069T= NCBI36
NG_011793.1:g.47382A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*38A= MANE Select ENSP00000233242.1:n.*38A=
ENST00000616098.4:c.13728A= ENSP00000477990.1:n.13728A=
NM_000384.2:c.*38A= NP_000375.2:n.*38A=
XM_011532809.1:c.5870-2419A= XP_011531111.1:n.5870-2419A=
NM_000384.3:c.*38A= MANE Select NP_000375.3:n.*38A=