Canonical Allele Identifier: CA2493482697
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023463C= , CM000664.2:g.21023463C= GRCh38
NC_000002.11:g.21246335C= , CM000664.1:g.21246335C= GRCh37
NC_000002.10:g.21099840C= NCBI36
NG_011793.1:g.25611G=

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*1910+62G= ENSP00000501110.2:n.*1910+62G=
ENST00000673882.2:c.*1910+62G= ENSP00000501253.2:n.*1910+62G=
ENST00000673739.1:c.2318+62G= ENSP00000501110.1:n.2318+62G=
ENST00000673882.1:c.2318+62G= ENSP00000501253.1:n.2318+62G=
ENST00000233242.5:c.2604+62G= MANE Select ENSP00000233242.1:n.2604+62G=
ENST00000616098.4:c.2604+62G= ENSP00000477990.1:n.2604+62G=
NM_000384.2:c.2604+62G= NP_000375.2:n.2604+62G=
XM_011532809.1:c.2604+62G= XP_011531111.1:n.2604+62G=
NM_000384.3:c.2604+62G= MANE Select NP_000375.3:n.2604+62G=