Canonical Allele Identifier: CA063818
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs746040932
ExAC: 2:21232806 C / T
gnomAD v2: 2-21232806-C-T
COSMIC: COSM1690254
MyVariant Identifiers: chr2:g.21232806C>T (hg19) chr2:g.21009934C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009934C>T , CM000664.2:g.21009934C>T GRCh38
NC_000002.11:g.21232806C>T , CM000664.1:g.21232806C>T GRCh37
NC_000002.10:g.21086311C>T NCBI36
NG_011793.1:g.39140G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6934G>A MANE Select ENSP00000233242.1:p.Asp2312Asn
ENST00000616098.4:c.6934G>A ENSP00000477990.1:p.Asp2312Asn
NM_000384.2:c.6934G>A NP_000375.2:p.Asp2312Asn
XM_011532809.1:c.5869+799G>A XP_011531111.1:n.5869+799G>A
NM_000384.3:c.6934G>A MANE Select NP_000375.3:p.Asp2312Asn
Search 100 bp 5'
Search 100 bp 3'