Canonical Allele Identifier: CA1345064145
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696099815
gnomAD v4: 3-10141573-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141573A>G , CM000665.2:g.10141573A>G GRCh38
NC_000003.11:g.10183257A>G , CM000665.1:g.10183257A>G GRCh37
NC_000003.10:g.10158257A>G NCBI36
NG_008212.3:g.4939A>G , LRG_322:g.4939A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-275A>G ENSP00000256474.2:n.-275A>G
Search 100 bp 5'
Search 100 bp 3'