Canonical Allele Identifier: CA2493476897
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010898_21010901delinsATTG , CM000664.2:g.21010898_21010901delinsATTG GRCh38
NC_000002.11:g.21233770_21233773delinsATTG , CM000664.1:g.21233770_21233773delinsATTG GRCh37
NC_000002.10:g.21087275_21087278delinsATTG NCBI36
NG_011793.1:g.38173_38176delinsCAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5967_5970delinsCAAT MANE Select ENSP00000233242.1:p.Asn1989=
ENST00000616098.4:c.5967_5970delinsCAAT ENSP00000477990.1:p.Asn1989=
NM_000384.2:c.5967_5970delinsCAAT NP_000375.2:p.Asn1989=
XM_011532809.1:c.5864+103_5864+106delinsCAAT XP_011531111.1:n.5864+103_5864+106delinsCAAT
NM_000384.3:c.5967_5970delinsCAAT MANE Select NP_000375.3:p.Asn1989=
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