Canonical Allele Identifier: CA2664399840
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141768del , CM000665.2:g.10141768del GRCh38
NC_000003.11:g.10183452del , CM000665.1:g.10183452del GRCh37
NC_000003.10:g.10158452del NCBI36
NG_008212.3:g.5134del , LRG_322:g.5134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-80del ENSP00000256474.2:n.-80del
NM_000551.3:c.-80del , LRG_322t1:c.-80del NP_000542.1:n.-80del
NM_198156.2:c.-80del NP_937799.1:n.-80del
XM_011534078.1:c.-80del XP_011532380.1:n.-80del
NM_001354723.1:c.-80del NP_001341652.1:n.-80del