Canonical Allele Identifier: CA345967957
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1662998868

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002152C>T , CM000664.2:g.21002152C>T GRCh38
NC_000002.11:g.21225024C>T , CM000664.1:g.21225024C>T GRCh37
NC_000002.10:g.21078529C>T NCBI36
NG_011793.1:g.46922G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13270G>A MANE Select ENSP00000233242.1:p.Glu4424Lys
ENST00000616098.4:c.13268G>A ENSP00000477990.1:n.13268G>A
NM_000384.2:c.13270G>A NP_000375.2:p.Glu4424Lys
XM_011532809.1:c.5870-2879G>A XP_011531111.1:n.5870-2879G>A
NM_000384.3:c.13270G>A MANE Select NP_000375.3:p.Glu4424Lys