Canonical Allele Identifier: CA2493475047
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006965T= , CM000664.2:g.21006965T= GRCh38
NC_000002.11:g.21229837T= , CM000664.1:g.21229837T= GRCh37
NC_000002.10:g.21083342T= NCBI36
NG_011793.1:g.42109A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9903A= MANE Select ENSP00000233242.1:p.Ser3301=
ENST00000616098.4:c.9903A= ENSP00000477990.1:p.Ser3301=
NM_000384.2:c.9903A= NP_000375.2:p.Ser3301=
XM_011532809.1:c.5869+3768A= XP_011531111.1:n.5869+3768A=
NM_000384.3:c.9903A= MANE Select NP_000375.3:p.Ser3301=