Canonical Allele Identifier: CA345987920
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006862T>G , CM000664.2:g.21006862T>G GRCh38
NC_000002.11:g.21229734T>G , CM000664.1:g.21229734T>G GRCh37
NC_000002.10:g.21083239T>G NCBI36
NG_011793.1:g.42212A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10006A>C MANE Select ENSP00000233242.1:p.Asn3336His
ENST00000616098.4:c.10006A>C ENSP00000477990.1:p.Asn3336His
NM_000384.2:c.10006A>C NP_000375.2:p.Asn3336His
XM_011532809.1:c.5869+3871A>C XP_011531111.1:n.5869+3871A>C
NM_000384.3:c.10006A>C MANE Select NP_000375.3:p.Asn3336His