Canonical Allele Identifier: CA896157242

Gene: VHL

Linked Data

• dbSNP Id: rs1362471337
• gnomAD v3: 3-10141548-AC-A
• gnomAD v4: 3-10141548-AC-A
• MyVariant Identifiers: chr3:g.10183233del (hg19) ; chr3:g.10141549del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141551del , CM000665.2:g.10141551del	GRCh38
NC_000003.11:g.10183235del , CM000665.1:g.10183235del	GRCh37
NC_000003.10:g.10158235del	NCBI36
NG_008212.3:g.4917del , LRG_322:g.4917del

Transcript Alleles

HGVS	Amino-acid change
ENST00000256474.2:c.-297del	ENSP00000256474.2:n.-297del