Canonical Allele Identifier: CA2698846982
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs2103352514
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006998del , CM000664.2:g.21006998del GRCh38
NC_000002.11:g.21229870del , CM000664.1:g.21229870del GRCh37
NC_000002.10:g.21083375del NCBI36
NG_011793.1:g.42077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9871del MANE Select ENSP00000233242.1:p.Arg3291ValfsTer7
ENST00000616098.4:c.9871del ENSP00000477990.1:p.Arg3291ValfsTer7
NM_000384.2:c.9871del NP_000375.2:p.Arg3291ValfsTer7
XM_011532809.1:c.5869+3736del XP_011531111.1:n.5869+3736del
NM_000384.3:c.9871del MANE Select NP_000375.3:p.Arg3291ValfsTer7
Search 100 bp 5'
Search 100 bp 3'