Canonical Allele Identifier: CA916488116
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1021877096
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21038333del , CM000664.2:g.21038333del GRCh38
NC_000002.11:g.21261205del , CM000664.1:g.21261205del GRCh37
NC_000002.10:g.21114710del NCBI36
NG_011793.1:g.10747del

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-1072del ENSP00000501110.2:n.384-1072del
ENST00000673882.2:c.384-1072del ENSP00000501253.2:n.384-1072del
ENST00000673739.1:c.252-1072del ENSP00000501110.1:n.252-1072del
ENST00000673882.1:c.252-1072del ENSP00000501253.1:n.252-1072del
ENST00000233242.5:c.384-216del MANE Select ENSP00000233242.1:n.384-216del
ENST00000399256.4:c.384-216del ENSP00000382200.4:n.384-216del
ENST00000616098.4:c.384-216del ENSP00000477990.1:n.384-216del
NM_000384.2:c.384-216del NP_000375.2:n.384-216del
XM_011532809.1:c.384-216del XP_011531111.1:n.384-216del
NM_000384.3:c.384-216del MANE Select NP_000375.3:n.384-216del
Search 100 bp 5'
Search 100 bp 3'