Canonical Allele Identifier: CA2664399506
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141558_10141559insCAA , CM000665.2:g.10141558_10141559insCAA GRCh38
NC_000003.11:g.10183242_10183243insCAA , CM000665.1:g.10183242_10183243insCAA GRCh37
NC_000003.10:g.10158242_10158243insCAA NCBI36
NG_008212.3:g.4924_4925insCAA , LRG_322:g.4924_4925insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-290_-289insCAA ENSP00000256474.2:n.-290_-289insCAA