Canonical Allele Identifier: CA346002351
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010671A>G , CM000664.2:g.21010671A>G GRCh38
NC_000002.11:g.21233543A>G , CM000664.1:g.21233543A>G GRCh37
NC_000002.10:g.21087048A>G NCBI36
NG_011793.1:g.38403T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6197T>C MANE Select ENSP00000233242.1:p.Val2066Ala
ENST00000616098.4:c.6197T>C ENSP00000477990.1:p.Val2066Ala
NM_000384.2:c.6197T>C NP_000375.2:p.Val2066Ala
XM_011532809.1:c.5869+62T>C XP_011531111.1:n.5869+62T>C
NM_000384.3:c.6197T>C MANE Select NP_000375.3:p.Val2066Ala