Canonical Allele Identifier: CA2493472913
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663004517
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002302_21002303del , CM000664.2:g.21002302_21002303del GRCh38
NC_000002.11:g.21225174_21225175del , CM000664.1:g.21225174_21225175del GRCh37
NC_000002.10:g.21078679_21078680del NCBI36
NG_011793.1:g.46771_46772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13119_13120del MANE Select ENSP00000233242.1:p.Glu4373AspfsTer13
ENST00000616098.4:c.13117_13118del ENSP00000477990.1:n.13117_13118del
NM_000384.2:c.13119_13120del NP_000375.2:p.Glu4373AspfsTer13
XM_011532809.1:c.5870-3030_5870-3029del XP_011531111.1:n.5870-3030_5870-3029del
NM_000384.3:c.13119_13120del MANE Select NP_000375.3:p.Glu4373AspfsTer13
Search 100 bp 5'
Search 100 bp 3'