Canonical Allele Identifier: CA2493482695
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023461A= , CM000664.2:g.21023461A= GRCh38
NC_000002.11:g.21246333A= , CM000664.1:g.21246333A= GRCh37
NC_000002.10:g.21099838A= NCBI36
NG_011793.1:g.25613T=

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*1910+64T= ENSP00000501110.2:n.*1910+64T=
ENST00000673882.2:c.*1910+64T= ENSP00000501253.2:n.*1910+64T=
ENST00000673739.1:c.2318+64T= ENSP00000501110.1:n.2318+64T=
ENST00000673882.1:c.2318+64T= ENSP00000501253.1:n.2318+64T=
ENST00000233242.5:c.2604+64T= MANE Select ENSP00000233242.1:n.2604+64T=
ENST00000616098.4:c.2604+64T= ENSP00000477990.1:n.2604+64T=
NM_000384.2:c.2604+64T= NP_000375.2:n.2604+64T=
XM_011532809.1:c.2604+64T= XP_011531111.1:n.2604+64T=
NM_000384.3:c.2604+64T= MANE Select NP_000375.3:n.2604+64T=