Canonical Allele Identifier: CA051998
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 402374
dbSNP Id: rs533755016
gnomAD v2: 2-21225140-C-T
gnomAD v3: 2-21002268-C-T
gnomAD v4: 2-21002268-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002268C>T , CM000664.2:g.21002268C>T GRCh38
NC_000002.11:g.21225140C>T , CM000664.1:g.21225140C>T GRCh37
NC_000002.10:g.21078645C>T NCBI36
NG_011793.1:g.46806G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.13154G>A MANE Select ENSP00000233242.1:p.Arg4385His
ENST00000616098.4:c.13152G>A ENSP00000477990.1:n.13152G>A
NM_000384.2:c.13154G>A NP_000375.2:p.Arg4385His
XM_011532809.1:c.5870-2995G>A XP_011531111.1:n.5870-2995G>A
NM_000384.3:c.13154G>A MANE Select NP_000375.3:p.Arg4385His