Canonical Allele Identifier: CA2755191066
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141439T>A , CM000665.2:g.10141439T>A GRCh38
NC_000003.11:g.10183123T>A , CM000665.1:g.10183123T>A GRCh37
NC_000003.10:g.10158123T>A NCBI36
NG_008212.3:g.4805T>A , LRG_322:g.4805T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-409T>A ENSP00000256474.2:n.-409T>A