Canonical Allele Identifier: CA2664399588
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141587-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141587G>A , CM000665.2:g.10141587G>A GRCh38
NC_000003.11:g.10183271G>A , CM000665.1:g.10183271G>A GRCh37
NC_000003.10:g.10158271G>A NCBI36
NG_008212.3:g.4953G>A , LRG_322:g.4953G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-261G>A ENSP00000256474.2:n.-261G>A