Canonical Allele Identifier: CA1345064021
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141488G= , CM000665.2:g.10141488G= GRCh38
NC_000003.11:g.10183172G= , CM000665.1:g.10183172G= GRCh37
NC_000003.10:g.10158172G= NCBI36
NG_008212.3:g.4854G= , LRG_322:g.4854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-360G= ENSP00000256474.2:n.-360G=