Canonical Allele Identifier: CA345988478
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1363244474
gnomAD v2: 2-21229886-A-T
gnomAD v3: 2-21007014-A-T
gnomAD v4: 2-21007014-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007014A>T , CM000664.2:g.21007014A>T GRCh38
NC_000002.11:g.21229886A>T , CM000664.1:g.21229886A>T GRCh37
NC_000002.10:g.21083391A>T NCBI36
NG_011793.1:g.42060T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9854T>A MANE Select ENSP00000233242.1:p.Ile3285Asn
ENST00000616098.4:c.9854T>A ENSP00000477990.1:p.Ile3285Asn
NM_000384.2:c.9854T>A NP_000375.2:p.Ile3285Asn
XM_011532809.1:c.5869+3719T>A XP_011531111.1:n.5869+3719T>A
NM_000384.3:c.9854T>A MANE Select NP_000375.3:p.Ile3285Asn