Canonical Allele Identifier: CA2493473111
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002727T= , CM000664.2:g.21002727T= GRCh38
NC_000002.11:g.21225599T= , CM000664.1:g.21225599T= GRCh37
NC_000002.10:g.21079104T= NCBI36
NG_011793.1:g.46347A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12695A= MANE Select ENSP00000233242.1:p.Tyr4232=
ENST00000616098.4:c.12695A= ENSP00000477990.1:p.Tyr4232=
NM_000384.2:c.12695A= NP_000375.2:p.Tyr4232=
XM_011532809.1:c.5870-3454A= XP_011531111.1:n.5870-3454A=
NM_000384.3:c.12695A= MANE Select NP_000375.3:p.Tyr4232=
Search 100 bp 5'
Search 100 bp 3'