Canonical Allele Identifier: CA1345064084
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141548A= , CM000665.2:g.10141548A= GRCh38
NC_000003.11:g.10183232A= , CM000665.1:g.10183232A= GRCh37
NC_000003.10:g.10158232A= NCBI36
NG_008212.3:g.4914A= , LRG_322:g.4914A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-300A= ENSP00000256474.2:n.-300A=