Canonical Allele Identifier: CA345986966
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21006631del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006631del , CM000664.2:g.21006631del GRCh38
NC_000002.11:g.21229503del , CM000664.1:g.21229503del GRCh37
NC_000002.10:g.21083008del NCBI36
NG_011793.1:g.42443del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10237del MANE Select ENSP00000233242.1:p.Thr3413LeufsTer2
ENST00000616098.4:c.10237del ENSP00000477990.1:p.Thr3413LeufsTer2
NM_000384.2:c.10237del NP_000375.2:p.Thr3413LeufsTer2
XM_011532809.1:c.5869+4102del XP_011531111.1:n.5869+4102del
NM_000384.3:c.10237del MANE Select NP_000375.3:p.Thr3413LeufsTer2
Search 100 bp 5'
Search 100 bp 3'