Canonical Allele Identifier: CA2749093803
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007005_21007006insTG , CM000664.2:g.21007005_21007006insTG GRCh38
NC_000002.11:g.21229877_21229878insTG , CM000664.1:g.21229877_21229878insTG GRCh37
NC_000002.10:g.21083382_21083383insTG NCBI36
NG_011793.1:g.42069_42070insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9863_9864insAC MANE Select ENSP00000233242.1:p.Asp3289LeufsTer10
ENST00000616098.4:c.9863_9864insAC ENSP00000477990.1:p.Asp3289LeufsTer10
NM_000384.2:c.9863_9864insAC NP_000375.2:p.Asp3289LeufsTer10
XM_011532809.1:c.5869+3728_5869+3729insAC XP_011531111.1:n.5869+3728_5869+3729insAC
NM_000384.3:c.9863_9864insAC MANE Select NP_000375.3:p.Asp3289LeufsTer10
Search 100 bp 5'
Search 100 bp 3'