Canonical Allele Identifier: CA1546524
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs769836306

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002625dup , CM000664.2:g.21002625dup GRCh38
NC_000002.11:g.21225497dup , CM000664.1:g.21225497dup GRCh37
NC_000002.10:g.21079002dup NCBI36
NG_011793.1:g.46449dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12797dup MANE Select ENSP00000233242.1:p.Ser4267LeufsTer4
ENST00000616098.4:c.12797dup ENSP00000477990.1:p.Ser4267LeufsTer4
NM_000384.2:c.12797dup NP_000375.2:p.Ser4267LeufsTer4
XM_011532809.1:c.5870-3352dup XP_011531111.1:n.5870-3352dup
NM_000384.3:c.12797dup MANE Select NP_000375.3:p.Ser4267LeufsTer4