Canonical Allele Identifier: CA1345064029
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141496T= , CM000665.2:g.10141496T= GRCh38
NC_000003.11:g.10183180T= , CM000665.1:g.10183180T= GRCh37
NC_000003.10:g.10158180T= NCBI36
NG_008212.3:g.4862T= , LRG_322:g.4862T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-352T= ENSP00000256474.2:n.-352T=