Canonical Allele Identifier: CA1345064102
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141556T= , CM000665.2:g.10141556T= GRCh38
NC_000003.11:g.10183240T= , CM000665.1:g.10183240T= GRCh37
NC_000003.10:g.10158240T= NCBI36
NG_008212.3:g.4922T= , LRG_322:g.4922T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-292T= ENSP00000256474.2:n.-292T=