Canonical Allele Identifier: CA2493474237
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005066_21005067delinsAG , CM000664.2:g.21005066_21005067delinsAG GRCh38
NC_000002.11:g.21227938_21227939delinsAG , CM000664.1:g.21227938_21227939delinsAG GRCh37
NC_000002.10:g.21081443_21081444delinsAG NCBI36
NG_011793.1:g.44007_44008delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11788+13_11788+14delinsCT MANE Select ENSP00000233242.1:n.11788+13_11788+14deli...
ENST00000616098.4:c.11788+13_11788+14delinsCT ENSP00000477990.1:n.11788+13_11788+14deli...
NM_000384.2:c.11788+13_11788+14delinsCT NP_000375.2:n.11788+13_11788+14delinsCT
XM_011532809.1:c.5869+5666_5869+5667delinsCT XP_011531111.1:n.5869+5666_5869+5667delin...
NM_000384.3:c.11788+13_11788+14delinsCT MANE Select NP_000375.3:n.11788+13_11788+14delinsCT
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