Canonical Allele Identifier: CA2493476288
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009553T= , CM000664.2:g.21009553T= GRCh38
NC_000002.11:g.21232425T= , CM000664.1:g.21232425T= GRCh37
NC_000002.10:g.21085930T= NCBI36
NG_011793.1:g.39521A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7315A= MANE Select ENSP00000233242.1:p.Thr2439=
ENST00000616098.4:c.7315A= ENSP00000477990.1:p.Thr2439=
NM_000384.2:c.7315A= NP_000375.2:p.Thr2439=
XM_011532809.1:c.5869+1180A= XP_011531111.1:n.5869+1180A=
NM_000384.3:c.7315A= MANE Select NP_000375.3:p.Thr2439=