Canonical Allele Identifier: CA2493474234
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005056G= , CM000664.2:g.21005056G= GRCh38
NC_000002.11:g.21227928G= , CM000664.1:g.21227928G= GRCh37
NC_000002.10:g.21081433G= NCBI36
NG_011793.1:g.44018C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11788+24C= MANE Select ENSP00000233242.1:n.11788+24C=
ENST00000616098.4:c.11788+24C= ENSP00000477990.1:n.11788+24C=
NM_000384.2:c.11788+24C= NP_000375.2:n.11788+24C=
XM_011532809.1:c.5869+5677C= XP_011531111.1:n.5869+5677C=
NM_000384.3:c.11788+24C= MANE Select NP_000375.3:n.11788+24C=
Search 100 bp 5'
Search 100 bp 3'