Canonical Allele Identifier: CA2493472886
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002254C= , CM000664.2:g.21002254C= GRCh38
NC_000002.11:g.21225126C= , CM000664.1:g.21225126C= GRCh37
NC_000002.10:g.21078631C= NCBI36
NG_011793.1:g.46820G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13168G= MANE Select ENSP00000233242.1:p.Asp4390=
ENST00000616098.4:c.13166G= ENSP00000477990.1:n.13166G=
NM_000384.2:c.13168G= NP_000375.2:p.Asp4390=
XM_011532809.1:c.5870-2981G= XP_011531111.1:n.5870-2981G=
NM_000384.3:c.13168G= MANE Select NP_000375.3:p.Asp4390=
Search 100 bp 5'
Search 100 bp 3'