Canonical Allele Identifier: CA2493476801
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010677T= , CM000664.2:g.21010677T= GRCh38
NC_000002.11:g.21233549T= , CM000664.1:g.21233549T= GRCh37
NC_000002.10:g.21087054T= NCBI36
NG_011793.1:g.38397A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6191A= MANE Select ENSP00000233242.1:p.Gln2064=
ENST00000616098.4:c.6191A= ENSP00000477990.1:p.Gln2064=
NM_000384.2:c.6191A= NP_000375.2:p.Gln2064=
XM_011532809.1:c.5869+56A= XP_011531111.1:n.5869+56A=
NM_000384.3:c.6191A= MANE Select NP_000375.3:p.Gln2064=