Canonical Allele Identifier: CA1345064213
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141626T= , CM000665.2:g.10141626T= GRCh38
NC_000003.11:g.10183310T= , CM000665.1:g.10183310T= GRCh37
NC_000003.10:g.10158310T= NCBI36
NG_008212.3:g.4992T= , LRG_322:g.4992T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-222T= ENSP00000256474.2:n.-222T=