Canonical Allele Identifier: CA2664399640
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141623dup , CM000665.2:g.10141623dup GRCh38
NC_000003.11:g.10183307dup , CM000665.1:g.10183307dup GRCh37
NC_000003.10:g.10158307dup NCBI36
NG_008212.3:g.4989dup , LRG_322:g.4989dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-225dup ENSP00000256474.2:n.-225dup