Canonical Allele Identifier: CA1345064079
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141544T= , CM000665.2:g.10141544T= GRCh38
NC_000003.11:g.10183228T= , CM000665.1:g.10183228T= GRCh37
NC_000003.10:g.10158228T= NCBI36
NG_008212.3:g.4910T= , LRG_322:g.4910T=

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-304T= ENSP00000256474.2:n.-304T=