Canonical Allele Identifier: CA2493472772
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1662994903
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002082_21002083insCC , CM000664.2:g.21002082_21002083insCC GRCh38
NC_000002.11:g.21224954_21224955insCC , CM000664.1:g.21224954_21224955insCC GRCh37
NC_000002.10:g.21078459_21078460insCC NCBI36
NG_011793.1:g.46991_46992insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13339_13340insGG MANE Select ENSP00000233242.1:p.Asn4447ArgfsTer31
ENST00000616098.4:c.13337_13338insGG ENSP00000477990.1:n.13337_13338insGG
NM_000384.2:c.13339_13340insGG NP_000375.2:p.Asn4447ArgfsTer31
XM_011532809.1:c.5870-2810_5870-2809insGG XP_011531111.1:n.5870-2810_5870-2809insGG
NM_000384.3:c.13339_13340insGG MANE Select NP_000375.3:p.Asn4447ArgfsTer31
Search 100 bp 5'
Search 100 bp 3'