Canonical Allele Identifier: CA2493474887
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006629_21006630delinsAG , CM000664.2:g.21006629_21006630delinsAG GRCh38
NC_000002.11:g.21229501_21229502delinsAG , CM000664.1:g.21229501_21229502delinsAG GRCh37
NC_000002.10:g.21083006_21083007delinsAG NCBI36
NG_011793.1:g.42444_42445delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10238_10239delinsCT MANE Select ENSP00000233242.1:p.Thr3413=
ENST00000616098.4:c.10238_10239delinsCT ENSP00000477990.1:p.Thr3413=
NM_000384.2:c.10238_10239delinsCT NP_000375.2:p.Thr3413=
XM_011532809.1:c.5869+4103_5869+4104delinsCT XP_011531111.1:n.5869+4103_5869+4104delinsCT
NM_000384.3:c.10238_10239delinsCT MANE Select NP_000375.3:p.Thr3413=
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