Canonical Allele Identifier: CA1345064099
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696098608

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141554_10141555insAA , CM000665.2:g.10141554_10141555insAA GRCh38
NC_000003.11:g.10183238_10183239insAA , CM000665.1:g.10183238_10183239insAA GRCh37
NC_000003.10:g.10158238_10158239insAA NCBI36
NG_008212.3:g.4920_4921insAA , LRG_322:g.4920_4921insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-294_-293insAA ENSP00000256474.2:n.-294_-293insAA