Canonical Allele Identifier: CA2493472804
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002127A= , CM000664.2:g.21002127A= GRCh38
NC_000002.11:g.21224999A= , CM000664.1:g.21224999A= GRCh37
NC_000002.10:g.21078504A= NCBI36
NG_011793.1:g.46947T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13295T= MANE Select ENSP00000233242.1:p.Phe4432=
ENST00000616098.4:c.13293T= ENSP00000477990.1:n.13293T=
NM_000384.2:c.13295T= NP_000375.2:p.Phe4432=
XM_011532809.1:c.5870-2854T= XP_011531111.1:n.5870-2854T=
NM_000384.3:c.13295T= MANE Select NP_000375.3:p.Phe4432=
Search 100 bp 5'
Search 100 bp 3'