Canonical Allele Identifier: CA2664399807
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141736_10141737del , CM000665.2:g.10141736_10141737del GRCh38
NC_000003.11:g.10183420_10183421del , CM000665.1:g.10183420_10183421del GRCh37
NC_000003.10:g.10158420_10158421del NCBI36
NG_008212.3:g.5102_5103del , LRG_322:g.5102_5103del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-112_-111del ENSP00000256474.2:n.-112_-111del
NM_000551.3:c.-112_-111del , LRG_322t1:c.-112_-111del NP_000542.1:n.-112_-111del
NM_198156.2:c.-112_-111del NP_937799.1:n.-112_-111del
NM_001354723.1:c.-112_-111del NP_001341652.1:n.-112_-111del