Canonical Allele Identifier: CA10613959
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334136
ClinVar RCV Id: RCV000295303 RCV000352545
dbSNP Id: rs886055585
MyVariant Identifiers: chr2:g.21234250G>C (hg19) chr2:g.21011378G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011378G>C , CM000664.2:g.21011378G>C GRCh38
NC_000002.11:g.21234250G>C , CM000664.1:g.21234250G>C GRCh37
NC_000002.10:g.21087755G>C NCBI36
NG_011793.1:g.37696C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*4796C>G ENSP00000501110.2:n.*4796C>G
ENST00000673739.1:c.5204C>G ENSP00000501110.1:n.5204C>G
ENST00000233242.5:c.5490C>G MANE Select ENSP00000233242.1:p.Ala1830=
ENST00000616098.4:c.5490C>G ENSP00000477990.1:p.Ala1830=
NM_000384.2:c.5490C>G NP_000375.2:p.Ala1830=
XM_011532809.1:c.5490C>G XP_011531111.1:p.Ala1830=
NM_000384.3:c.5490C>G MANE Select NP_000375.3:p.Ala1830=
Search 100 bp 5'
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