Canonical Allele Identifier: CA2664399505
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141557_10141558insCAA , CM000665.2:g.10141557_10141558insCAA GRCh38
NC_000003.11:g.10183241_10183242insCAA , CM000665.1:g.10183241_10183242insCAA GRCh37
NC_000003.10:g.10158241_10158242insCAA NCBI36
NG_008212.3:g.4923_4924insCAA , LRG_322:g.4923_4924insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-291_-290insCAA ENSP00000256474.2:n.-291_-290insCAA