Canonical Allele Identifier: CA345968173
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663000544
gnomAD v4: 2-21002184-T-G
MyVariant Identifiers: chr2:g.21225056T>G (hg19) chr2:g.21002184T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002184T>G , CM000664.2:g.21002184T>G GRCh38
NC_000002.11:g.21225056T>G , CM000664.1:g.21225056T>G GRCh37
NC_000002.10:g.21078561T>G NCBI36
NG_011793.1:g.46890A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13238A>C MANE Select ENSP00000233242.1:p.Asn4413Thr
ENST00000616098.4:c.13236A>C ENSP00000477990.1:n.13236A>C
NM_000384.2:c.13238A>C NP_000375.2:p.Asn4413Thr
XM_011532809.1:c.5870-2911A>C XP_011531111.1:n.5870-2911A>C
NM_000384.3:c.13238A>C MANE Select NP_000375.3:p.Asn4413Thr
Search 100 bp 5'
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