Canonical Allele Identifier: CA2576686432

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21001723T>C , CM000664.2:g.21001723T>C	GRCh38
NC_000002.11:g.21224595T>C , CM000664.1:g.21224595T>C	GRCh37
NC_000002.10:g.21078100T>C	NCBI36
NG_011793.1:g.47351A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.*7A>G MANE Select	ENSP00000233242.1:n.*7A>G
ENST00000616098.4:c.13697A>G	ENSP00000477990.1:n.13697A>G
NM_000384.2:c.*7A>G	NP_000375.2:n.*7A>G
XM_011532809.1:c.5870-2450A>G	XP_011531111.1:n.5870-2450A>G
NM_000384.3:c.*7A>G MANE Select	NP_000375.3:n.*7A>G