Canonical Allele Identifier: CA1345063980
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141438G= , CM000665.2:g.10141438G= GRCh38
NC_000003.11:g.10183122G= , CM000665.1:g.10183122G= GRCh37
NC_000003.10:g.10158122G= NCBI36
NG_008212.3:g.4804G= , LRG_322:g.4804G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-410G= ENSP00000256474.2:n.-410G=