Canonical Allele Identifier: CA345969628
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002368G>T , CM000664.2:g.21002368G>T GRCh38
NC_000002.11:g.21225240G>T , CM000664.1:g.21225240G>T GRCh37
NC_000002.10:g.21078745G>T NCBI36
NG_011793.1:g.46706C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13054C>A MANE Select ENSP00000233242.1:p.Leu4352Ile
ENST00000616098.4:c.13052C>A ENSP00000477990.1:n.13052C>A
NM_000384.2:c.13054C>A NP_000375.2:p.Leu4352Ile
XM_011532809.1:c.5870-3095C>A XP_011531111.1:n.5870-3095C>A
NM_000384.3:c.13054C>A MANE Select NP_000375.3:p.Leu4352Ile