Canonical Allele Identifier: CA346004498
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011326A>C , CM000664.2:g.21011326A>C GRCh38
NC_000002.11:g.21234198A>C , CM000664.1:g.21234198A>C GRCh37
NC_000002.10:g.21087703A>C NCBI36
NG_011793.1:g.37748T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5542T>G MANE Select ENSP00000233242.1:p.Ser1848Ala
ENST00000616098.4:c.5542T>G ENSP00000477990.1:p.Ser1848Ala
NM_000384.2:c.5542T>G NP_000375.2:p.Ser1848Ala
XM_011532809.1:c.5542T>G XP_011531111.1:p.Ser1848Ala
NM_000384.3:c.5542T>G MANE Select NP_000375.3:p.Ser1848Ala