Canonical Allele Identifier: CA2493472774
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002085_21002087delinsCTG , CM000664.2:g.21002085_21002087delinsCTG GRCh38
NC_000002.11:g.21224957_21224959delinsCTG , CM000664.1:g.21224957_21224959delinsCTG GRCh37
NC_000002.10:g.21078462_21078464delinsCTG NCBI36
NG_011793.1:g.46987_46989delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13335_13337delinsCAG MANE Select ENSP00000233242.1:p.His4445=
ENST00000616098.4:c.13333_13335delinsCAG ENSP00000477990.1:n.13333_13335delinsCAG
NM_000384.2:c.13335_13337delinsCAG NP_000375.2:p.His4445=
XM_011532809.1:c.5870-2814_5870-2812delinsCAG XP_011531111.1:n.5870-2814_5870-2812delinsCAG
NM_000384.3:c.13335_13337delinsCAG MANE Select NP_000375.3:p.His4445=
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