Canonical Allele Identifier: CA2702129697
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs2125123915
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141456G>T , CM000665.2:g.10141456G>T GRCh38
NC_000003.11:g.10183140G>T , CM000665.1:g.10183140G>T GRCh37
NC_000003.10:g.10158140G>T NCBI36
NG_008212.3:g.4822G>T , LRG_322:g.4822G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-392G>T ENSP00000256474.2:n.-392G>T
Search 100 bp 5'
Search 100 bp 3'