Canonical Allele Identifier: CA346002185
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21010625-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010625A>T , CM000664.2:g.21010625A>T GRCh38
NC_000002.11:g.21233497A>T , CM000664.1:g.21233497A>T GRCh37
NC_000002.10:g.21087002A>T NCBI36
NG_011793.1:g.38449T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6243T>A MANE Select ENSP00000233242.1:p.Phe2081Leu
ENST00000616098.4:c.6243T>A ENSP00000477990.1:p.Phe2081Leu
NM_000384.2:c.6243T>A NP_000375.2:p.Phe2081Leu
XM_011532809.1:c.5869+108T>A XP_011531111.1:n.5869+108T>A
NM_000384.3:c.6243T>A MANE Select NP_000375.3:p.Phe2081Leu