Canonical Allele Identifier: CA050765
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs748744377
gnomAD v2: 2-21225654-C-T
gnomAD v4: 2-21002782-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002782C>T , CM000664.2:g.21002782C>T GRCh38
NC_000002.11:g.21225654C>T , CM000664.1:g.21225654C>T GRCh37
NC_000002.10:g.21079159C>T NCBI36
NG_011793.1:g.46292G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.12640G>A MANE Select ENSP00000233242.1:p.Glu4214Lys
ENST00000616098.4:c.12640G>A ENSP00000477990.1:p.Glu4214Lys
NM_000384.2:c.12640G>A NP_000375.2:p.Glu4214Lys
XM_011532809.1:c.5870-3509G>A XP_011531111.1:n.5870-3509G>A
NM_000384.3:c.12640G>A MANE Select NP_000375.3:p.Glu4214Lys