Canonical Allele Identifier: CA896157236

Gene: VHL

Linked Data

• dbSNP Id: rs1277796230
• gnomAD v4: 3-10141547-G-T
• MyVariant Identifiers: chr3:g.10183231G>T (hg19) ; chr3:g.10141547G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141547G>T , CM000665.2:g.10141547G>T	GRCh38
NC_000003.11:g.10183231G>T , CM000665.1:g.10183231G>T	GRCh37
NC_000003.10:g.10158231G>T	NCBI36
NG_008212.3:g.4913G>T , LRG_322:g.4913G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000256474.2:c.-301G>T	ENSP00000256474.2:n.-301G>T