Canonical Allele Identifier: CA2658056055
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010538_21010546del , CM000664.2:g.21010538_21010546del GRCh38
NC_000002.11:g.21233410_21233418del , CM000664.1:g.21233410_21233418del GRCh37
NC_000002.10:g.21086915_21086923del NCBI36
NG_011793.1:g.38528_38536del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6322_6330del MANE Select ENSP00000233242.1:p.Val2108_Lys2110del
ENST00000616098.4:c.6322_6330del ENSP00000477990.1:p.Val2108_Lys2110del
NM_000384.2:c.6322_6330del NP_000375.2:p.Val2108_Lys2110del
XM_011532809.1:c.5869+187_5869+195del XP_011531111.1:n.5869+187_5869+195del
NM_000384.3:c.6322_6330del MANE Select NP_000375.3:p.Val2108_Lys2110del