Canonical Allele Identifier: CA2493476563
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010140C= , CM000664.2:g.21010140C= GRCh38
NC_000002.11:g.21233012C= , CM000664.1:g.21233012C= GRCh37
NC_000002.10:g.21086517C= NCBI36
NG_011793.1:g.38934G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6728G= MANE Select ENSP00000233242.1:p.Ser2243=
ENST00000616098.4:c.6728G= ENSP00000477990.1:p.Ser2243=
NM_000384.2:c.6728G= NP_000375.2:p.Ser2243=
XM_011532809.1:c.5869+593G= XP_011531111.1:n.5869+593G=
NM_000384.3:c.6728G= MANE Select NP_000375.3:p.Ser2243=