Canonical Allele Identifier: CA346000655
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010054G>C , CM000664.2:g.21010054G>C GRCh38
NC_000002.11:g.21232926G>C , CM000664.1:g.21232926G>C GRCh37
NC_000002.10:g.21086431G>C NCBI36
NG_011793.1:g.39020C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6814C>G MANE Select ENSP00000233242.1:p.His2272Asp
ENST00000616098.4:c.6814C>G ENSP00000477990.1:p.His2272Asp
NM_000384.2:c.6814C>G NP_000375.2:p.His2272Asp
XM_011532809.1:c.5869+679C>G XP_011531111.1:n.5869+679C>G
NM_000384.3:c.6814C>G MANE Select NP_000375.3:p.His2272Asp