Canonical Allele Identifier: CA1044994389
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141556del , CM000665.2:g.10141556del GRCh38
NC_000003.11:g.10183240del , CM000665.1:g.10183240del GRCh37
NC_000003.10:g.10158240del NCBI36
NG_008212.3:g.4922del , LRG_322:g.4922del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-292del ENSP00000256474.2:n.-292del