Canonical Allele Identifier: CA2493476862
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010813G= , CM000664.2:g.21010813G= GRCh38
NC_000002.11:g.21233685G= , CM000664.1:g.21233685G= GRCh37
NC_000002.10:g.21087190G= NCBI36
NG_011793.1:g.38261C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6055C= MANE Select ENSP00000233242.1:p.Leu2019=
ENST00000616098.4:c.6055C= ENSP00000477990.1:p.Leu2019=
NM_000384.2:c.6055C= NP_000375.2:p.Leu2019=
XM_011532809.1:c.5865-76C= XP_011531111.1:n.5865-76C=
NM_000384.3:c.6055C= MANE Select NP_000375.3:p.Leu2019=
Search 100 bp 5'
Search 100 bp 3'