Canonical Allele Identifier: CA2493476893
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010888G= , CM000664.2:g.21010888G= GRCh38
NC_000002.11:g.21233760G= , CM000664.1:g.21233760G= GRCh37
NC_000002.10:g.21087265G= NCBI36
NG_011793.1:g.38186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5980C= MANE Select ENSP00000233242.1:p.Gln1994=
ENST00000616098.4:c.5980C= ENSP00000477990.1:p.Gln1994=
NM_000384.2:c.5980C= NP_000375.2:p.Gln1994=
XM_011532809.1:c.5864+116C= XP_011531111.1:n.5864+116C=
NM_000384.3:c.5980C= MANE Select NP_000375.3:p.Gln1994=