Canonical Allele Identifier: CA2493475069
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007010_21007011delinsTA , CM000664.2:g.21007010_21007011delinsTA GRCh38
NC_000002.11:g.21229882_21229883delinsTA , CM000664.1:g.21229882_21229883delinsTA GRCh37
NC_000002.10:g.21083387_21083388delinsTA NCBI36
NG_011793.1:g.42063_42064delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9857_9858delinsTA MANE Select ENSP00000233242.1:p.Leu3286=
ENST00000616098.4:c.9857_9858delinsTA ENSP00000477990.1:p.Leu3286=
NM_000384.2:c.9857_9858delinsTA NP_000375.2:p.Leu3286=
XM_011532809.1:c.5869+3722_5869+3723delinsTA XP_011531111.1:n.5869+3722_5869+3723delinsTA
NM_000384.3:c.9857_9858delinsTA MANE Select NP_000375.3:p.Leu3286=
Search 100 bp 5'
Search 100 bp 3'