Canonical Allele Identifier: CA345997553
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009610G>T , CM000664.2:g.21009610G>T GRCh38
NC_000002.11:g.21232482G>T , CM000664.1:g.21232482G>T GRCh37
NC_000002.10:g.21085987G>T NCBI36
NG_011793.1:g.39464C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7258C>A MANE Select ENSP00000233242.1:p.Leu2420Ile
ENST00000616098.4:c.7258C>A ENSP00000477990.1:p.Leu2420Ile
NM_000384.2:c.7258C>A NP_000375.2:p.Leu2420Ile
XM_011532809.1:c.5869+1123C>A XP_011531111.1:n.5869+1123C>A
NM_000384.3:c.7258C>A MANE Select NP_000375.3:p.Leu2420Ile