Canonical Allele Identifier: CA1345064398
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696106631
gnomAD v4: 3-10141729-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141729T>A , CM000665.2:g.10141729T>A GRCh38
NC_000003.11:g.10183413T>A , CM000665.1:g.10183413T>A GRCh37
NC_000003.10:g.10158413T>A NCBI36
NG_008212.3:g.5095T>A , LRG_322:g.5095T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-119T>A ENSP00000256474.2:n.-119T>A
NM_000551.3:c.-119T>A , LRG_322t1:c.-119T>A NP_000542.1:n.-119T>A
NM_198156.2:c.-119T>A NP_937799.1:n.-119T>A
NM_001354723.1:c.-119T>A NP_001341652.1:n.-119T>A
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