Canonical Allele Identifier: CA425346073
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233779A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010907A>G , CM000664.2:g.21010907A>G GRCh38
NC_000002.11:g.21233779A>G , CM000664.1:g.21233779A>G GRCh37
NC_000002.10:g.21087284A>G NCBI36
NG_011793.1:g.38167T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5961T>C MANE Select ENSP00000233242.1:p.Phe1987=
ENST00000616098.4:c.5961T>C ENSP00000477990.1:p.Phe1987=
NM_000384.2:c.5961T>C NP_000375.2:p.Phe1987=
XM_011532809.1:c.5864+97T>C XP_011531111.1:n.5864+97T>C
NM_000384.3:c.5961T>C MANE Select NP_000375.3:p.Phe1987=
Search 100 bp 5'
Search 100 bp 3'