Canonical Allele Identifier: CA066576
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334113
dbSNP Id: rs13306196

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007391C>T , CM000664.2:g.21007391C>T GRCh38
NC_000002.11:g.21230263C>T , CM000664.1:g.21230263C>T GRCh37
NC_000002.10:g.21083768C>T NCBI36
NG_011793.1:g.41683G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.9477G>A MANE Select ENSP00000233242.1:p.Lys3159=
ENST00000616098.4:n.9477G>A ENSP00000477990.1:p.Lys3159=
NM_000384.2:c.9477G>A NP_000375.2:p.Lys3159=
XM_011532809.1:c.5869+3342G>A XP_011531111.1:p.=
NM_000384.3:c.9477G>A MANE Select NP_000375.3:p.Lys3159=