Canonical Allele Identifier: CA1345064089
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141549C= , CM000665.2:g.10141549C= GRCh38
NC_000003.11:g.10183233C= , CM000665.1:g.10183233C= GRCh37
NC_000003.10:g.10158233C= NCBI36
NG_008212.3:g.4915C= , LRG_322:g.4915C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-299C= ENSP00000256474.2:n.-299C=