Canonical Allele Identifier: CA1345064101
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696098668

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141555_10141556insAA , CM000665.2:g.10141555_10141556insAA GRCh38
NC_000003.11:g.10183239_10183240insAA , CM000665.1:g.10183239_10183240insAA GRCh37
NC_000003.10:g.10158239_10158240insAA NCBI36
NG_008212.3:g.4921_4922insAA , LRG_322:g.4921_4922insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-293_-292insAA ENSP00000256474.2:n.-293_-292insAA