Canonical Allele Identifier: CA050565
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 757138
ClinVar RCV Id: RCV001838306
dbSNP Id: rs752965923
ExAC: 2:21225733 C / T
gnomAD v2: 2-21225733-C-T
gnomAD v4: 2-21002861-C-T
MyVariant Identifiers: chr2:g.21225733C>T (hg19) chr2:g.21002861C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002861C>T , CM000664.2:g.21002861C>T GRCh38
NC_000002.11:g.21225733C>T , CM000664.1:g.21225733C>T GRCh37
NC_000002.10:g.21079238C>T NCBI36
NG_011793.1:g.46213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12561G>A MANE Select ENSP00000233242.1:p.Lys4187=
ENST00000616098.4:c.12561G>A ENSP00000477990.1:p.Lys4187=
NM_000384.2:c.12561G>A NP_000375.2:p.Lys4187=
XM_011532809.1:c.5870-3588G>A XP_011531111.1:n.5870-3588G>A
NM_000384.3:c.12561G>A MANE Select NP_000375.3:p.Lys4187=
Search 100 bp 5'
Search 100 bp 3'