Canonical Allele Identifier: CA345987338
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 579092
ClinVar RCV Id: RCV001838112
dbSNP Id: rs1558561585
MyVariant Identifiers: chr2:g.21229594C>G (hg19) chr2:g.21006722C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006722C>G , CM000664.2:g.21006722C>G GRCh38
NC_000002.11:g.21229594C>G , CM000664.1:g.21229594C>G GRCh37
NC_000002.10:g.21083099C>G NCBI36
NG_011793.1:g.42352G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10146G>C MANE Select ENSP00000233242.1:p.Glu3382Asp
ENST00000616098.4:c.10146G>C ENSP00000477990.1:p.Glu3382Asp
NM_000384.2:c.10146G>C NP_000375.2:p.Glu3382Asp
XM_011532809.1:c.5869+4011G>C XP_011531111.1:n.5869+4011G>C
NM_000384.3:c.10146G>C MANE Select NP_000375.3:p.Glu3382Asp
Search 100 bp 5'
Search 100 bp 3'