Canonical Allele Identifier: CA2664399511
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141560-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141560A>G , CM000665.2:g.10141560A>G GRCh38
NC_000003.11:g.10183244A>G , CM000665.1:g.10183244A>G GRCh37
NC_000003.10:g.10158244A>G NCBI36
NG_008212.3:g.4926A>G , LRG_322:g.4926A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-288A>G ENSP00000256474.2:n.-288A>G