Canonical Allele Identifier: CA345968740
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002248T>A , CM000664.2:g.21002248T>A GRCh38
NC_000002.11:g.21225120T>A , CM000664.1:g.21225120T>A GRCh37
NC_000002.10:g.21078625T>A NCBI36
NG_011793.1:g.46826A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13174A>T MANE Select ENSP00000233242.1:p.Ser4392Cys
ENST00000616098.4:c.13172A>T ENSP00000477990.1:n.13172A>T
NM_000384.2:c.13174A>T NP_000375.2:p.Ser4392Cys
XM_011532809.1:c.5870-2975A>T XP_011531111.1:n.5870-2975A>T
NM_000384.3:c.13174A>T MANE Select NP_000375.3:p.Ser4392Cys