Canonical Allele Identifier: CA2493473802
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005216_21005218delinsAGT , CM000664.2:g.21005216_21005218delinsAGT GRCh38
NC_000002.11:g.21228088_21228090delinsAGT , CM000664.1:g.21228088_21228090delinsAGT GRCh37
NC_000002.10:g.21081593_21081595delinsAGT NCBI36
NG_011793.1:g.43856_43858delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.11650_11652delinsACT MANE Select ENSP00000233242.1:p.Thr3884=
ENST00000616098.4:c.11650_11652delinsACT ENSP00000477990.1:p.Thr3884=
NM_000384.2:c.11650_11652delinsACT NP_000375.2:p.Thr3884=
XM_011532809.1:c.5869+5515_5869+5517delinsACT XP_011531111.1:n.5869+5515_5869+5517delinsACT
NM_000384.3:c.11650_11652delinsACT MANE Select NP_000375.3:p.Thr3884=
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