Canonical Allele Identifier: CA2658054413
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21001695-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001699del , CM000664.2:g.21001699del GRCh38
NC_000002.11:g.21224571del , CM000664.1:g.21224571del GRCh37
NC_000002.10:g.21078076del NCBI36
NG_011793.1:g.47378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*34del MANE Select ENSP00000233242.1:n.*34del
ENST00000616098.4:c.13724del ENSP00000477990.1:n.13724del
NM_000384.2:c.*34del NP_000375.2:n.*34del
XM_011532809.1:c.5870-2423del XP_011531111.1:n.5870-2423del
NM_000384.3:c.*34del MANE Select NP_000375.3:n.*34del
Search 100 bp 5'
Search 100 bp 3'