Canonical Allele Identifier: CA2493476582
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010187A= , CM000664.2:g.21010187A= GRCh38
NC_000002.11:g.21233059A= , CM000664.1:g.21233059A= GRCh37
NC_000002.10:g.21086564A= NCBI36
NG_011793.1:g.38887T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6681T= MANE Select ENSP00000233242.1:p.His2227=
ENST00000616098.4:c.6681T= ENSP00000477990.1:p.His2227=
NM_000384.2:c.6681T= NP_000375.2:p.His2227=
XM_011532809.1:c.5869+546T= XP_011531111.1:n.5869+546T=
NM_000384.3:c.6681T= MANE Select NP_000375.3:p.His2227=