Canonical Allele Identifier: CA70041946

Gene: VHL

Linked Data

• dbSNP Id: rs966617640
• gnomAD v4: 3-10141758-G-A
• MyVariant Identifiers: chr3:g.10183442G>A (hg19) ; chr3:g.10141758G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141758G>A , CM000665.2:g.10141758G>A	GRCh38
NC_000003.11:g.10183442G>A , CM000665.1:g.10183442G>A	GRCh37
NC_000003.10:g.10158442G>A	NCBI36
NG_008212.3:g.5124G>A , LRG_322:g.5124G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256474.2:c.-90G>A	ENSP00000256474.2:n.-90G>A
NM_000551.3:c.-90G>A , LRG_322t1:c.-90G>A	NP_000542.1:n.-90G>A
NM_198156.2:c.-90G>A	NP_937799.1:n.-90G>A
NM_001354723.1:c.-90G>A	NP_001341652.1:n.-90G>A