Canonical Allele Identifier: CA345968931
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21225146G>T (hg19) chr2:g.21002274G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002274G>T , CM000664.2:g.21002274G>T GRCh38
NC_000002.11:g.21225146G>T , CM000664.1:g.21225146G>T GRCh37
NC_000002.10:g.21078651G>T NCBI36
NG_011793.1:g.46800C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13148C>A MANE Select ENSP00000233242.1:p.Ala4383Asp
ENST00000616098.4:c.13146C>A ENSP00000477990.1:n.13146C>A
NM_000384.2:c.13148C>A NP_000375.2:p.Ala4383Asp
XM_011532809.1:c.5870-3001C>A XP_011531111.1:n.5870-3001C>A
NM_000384.3:c.13148C>A MANE Select NP_000375.3:p.Ala4383Asp
Search 100 bp 5'
Search 100 bp 3'