Canonical Allele Identifier: CA346004459
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011308C>A , CM000664.2:g.21011308C>A GRCh38
NC_000002.11:g.21234180C>A , CM000664.1:g.21234180C>A GRCh37
NC_000002.10:g.21087685C>A NCBI36
NG_011793.1:g.37766G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5560G>T MANE Select ENSP00000233242.1:p.Asp1854Tyr
ENST00000616098.4:c.5560G>T ENSP00000477990.1:p.Asp1854Tyr
NM_000384.2:c.5560G>T NP_000375.2:p.Asp1854Tyr
XM_011532809.1:c.5560G>T XP_011531111.1:p.Asp1854Tyr
NM_000384.3:c.5560G>T MANE Select NP_000375.3:p.Asp1854Tyr