Canonical Allele Identifier: CA1345064105
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696098774

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141556_10141557insAAAA , CM000665.2:g.10141556_10141557insAAAA GRCh38
NC_000003.11:g.10183240_10183241insAAAA , CM000665.1:g.10183240_10183241insAAAA GRCh37
NC_000003.10:g.10158240_10158241insAAAA NCBI36
NG_008212.3:g.4922_4923insAAAA , LRG_322:g.4922_4923insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-292_-291insAAAA ENSP00000256474.2:n.-292_-291insAAAA