Canonical Allele Identifier: CA1345064279
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696102885
gnomAD v4: 3-10141655-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141655C>A , CM000665.2:g.10141655C>A GRCh38
NC_000003.11:g.10183339C>A , CM000665.1:g.10183339C>A GRCh37
NC_000003.10:g.10158339C>A NCBI36
NG_008212.3:g.5021C>A , LRG_322:g.5021C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-193C>A ENSP00000256474.2:n.-193C>A
NM_000551.3:c.-193C>A , LRG_322t1:c.-193C>A NP_000542.1:n.-193C>A
NM_198156.2:c.-193C>A NP_937799.1:n.-193C>A
NM_001354723.1:c.-193C>A NP_001341652.1:n.-193C>A