Canonical Allele Identifier: CA1345064090
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141550C= , CM000665.2:g.10141550C= GRCh38
NC_000003.11:g.10183234C= , CM000665.1:g.10183234C= GRCh37
NC_000003.10:g.10158234C= NCBI36
NG_008212.3:g.4916C= , LRG_322:g.4916C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-298C= ENSP00000256474.2:n.-298C=