Canonical Allele Identifier: CA916488022
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1572783957
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010985_21010986del , CM000664.2:g.21010985_21010986del GRCh38
NC_000002.11:g.21233857_21233858del , CM000664.1:g.21233857_21233858del GRCh37
NC_000002.10:g.21087362_21087363del NCBI36
NG_011793.1:g.38089_38090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5883_5884del MANE Select ENSP00000233242.1:p.Ala1962SerfsTer3
ENST00000616098.4:c.5883_5884del ENSP00000477990.1:p.Ala1962SerfsTer3
NM_000384.2:c.5883_5884del NP_000375.2:p.Ala1962SerfsTer3
XM_011532809.1:c.5864+19_5864+20del XP_011531111.1:n.5864+19_5864+20del
NM_000384.3:c.5883_5884del MANE Select NP_000375.3:p.Ala1962SerfsTer3
Search 100 bp 5'
Search 100 bp 3'