Canonical Allele Identifier: CA2493472633
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001822_21001823delinsAT , CM000664.2:g.21001822_21001823delinsAT GRCh38
NC_000002.11:g.21224694_21224695delinsAT , CM000664.1:g.21224694_21224695delinsAT GRCh37
NC_000002.10:g.21078199_21078200delinsAT NCBI36
NG_011793.1:g.47251_47252delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13599_13600delinsAT MANE Select ENSP00000233242.1:p.Ile4533=
ENST00000616098.4:c.13597_13598delinsAT ENSP00000477990.1:n.13597_13598delinsAT
NM_000384.2:c.13599_13600delinsAT NP_000375.2:p.Ile4533=
XM_011532809.1:c.5870-2550_5870-2549delinsAT XP_011531111.1:n.5870-2550_5870-2549delinsAT
NM_000384.3:c.13599_13600delinsAT MANE Select NP_000375.3:p.Ile4533=
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