Canonical Allele Identifier: CA2493472961
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002396_21002397delinsTG , CM000664.2:g.21002396_21002397delinsTG GRCh38
NC_000002.11:g.21225268_21225269delinsTG , CM000664.1:g.21225268_21225269delinsTG GRCh37
NC_000002.10:g.21078773_21078774delinsTG NCBI36
NG_011793.1:g.46677_46678delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13025_13026delinsCA MANE Select ENSP00000233242.1:p.Pro4342=
ENST00000616098.4:c.13025_13026delinsCA ENSP00000477990.1:p.Pro4342=
NM_000384.2:c.13025_13026delinsCA NP_000375.2:p.Pro4342=
XM_011532809.1:c.5870-3124_5870-3123delinsCA XP_011531111.1:n.5870-3124_5870-3123delinsCA
NM_000384.3:c.13025_13026delinsCA MANE Select NP_000375.3:p.Pro4342=
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