Canonical Allele Identifier: CA2664399557
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141575-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141575C>G , CM000665.2:g.10141575C>G GRCh38
NC_000003.11:g.10183259C>G , CM000665.1:g.10183259C>G GRCh37
NC_000003.10:g.10158259C>G NCBI36
NG_008212.3:g.4941C>G , LRG_322:g.4941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-273C>G ENSP00000256474.2:n.-273C>G