Canonical Allele Identifier: CA1345064103
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141557C= , CM000665.2:g.10141557C= GRCh38
NC_000003.11:g.10183241C= , CM000665.1:g.10183241C= GRCh37
NC_000003.10:g.10158241C= NCBI36
NG_008212.3:g.4923C= , LRG_322:g.4923C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-291C= ENSP00000256474.2:n.-291C=