Canonical Allele Identifier: CA2493472847
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002195_21002196delinsAC , CM000664.2:g.21002195_21002196delinsAC GRCh38
NC_000002.11:g.21225067_21225068delinsAC , CM000664.1:g.21225067_21225068delinsAC GRCh37
NC_000002.10:g.21078572_21078573delinsAC NCBI36
NG_011793.1:g.46878_46879delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13226_13227delinsGT MANE Select ENSP00000233242.1:p.Ser4409=
ENST00000616098.4:c.13224_13225delinsGT ENSP00000477990.1:n.13224_13225delinsGT
NM_000384.2:c.13226_13227delinsGT NP_000375.2:p.Ser4409=
XM_011532809.1:c.5870-2923_5870-2922delinsGT XP_011531111.1:n.5870-2923_5870-2922delinsGT
NM_000384.3:c.13226_13227delinsGT MANE Select NP_000375.3:p.Ser4409=
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