Canonical Allele Identifier: CA2493476955
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011011_21011012delinsGA , CM000664.2:g.21011011_21011012delinsGA GRCh38
NC_000002.11:g.21233883_21233884delinsGA , CM000664.1:g.21233883_21233884delinsGA GRCh37
NC_000002.10:g.21087388_21087389delinsGA NCBI36
NG_011793.1:g.38062_38063delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5856_5857delinsTC MANE Select ENSP00000233242.1:p.His1952=
ENST00000616098.4:c.5856_5857delinsTC ENSP00000477990.1:p.His1952=
NM_000384.2:c.5856_5857delinsTC NP_000375.2:p.His1952=
XM_011532809.1:c.5856_5857delinsTC XP_011531111.1:p.His1952=
NM_000384.3:c.5856_5857delinsTC MANE Select NP_000375.3:p.His1952=
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