Canonical Allele Identifier: CA2576686486

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21005073T>C , CM000664.2:g.21005073T>C	GRCh38
NC_000002.11:g.21227945T>C , CM000664.1:g.21227945T>C	GRCh37
NC_000002.10:g.21081450T>C	NCBI36
NG_011793.1:g.44001A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.11788+7A>G MANE Select	ENSP00000233242.1:n.11788+7A>G
ENST00000616098.4:c.11788+7A>G	ENSP00000477990.1:n.11788+7A>G
NM_000384.2:c.11788+7A>G	NP_000375.2:n.11788+7A>G
XM_011532809.1:c.5869+5660A>G	XP_011531111.1:n.5869+5660A>G
NM_000384.3:c.11788+7A>G MANE Select	NP_000375.3:n.11788+7A>G