Canonical Allele Identifier: CA2664399825
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141749-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141749A>G , CM000665.2:g.10141749A>G GRCh38
NC_000003.11:g.10183433A>G , CM000665.1:g.10183433A>G GRCh37
NC_000003.10:g.10158433A>G NCBI36
NG_008212.3:g.5115A>G , LRG_322:g.5115A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-99A>G ENSP00000256474.2:n.-99A>G
NM_000551.3:c.-99A>G , LRG_322t1:c.-99A>G NP_000542.1:n.-99A>G
NM_198156.2:c.-99A>G NP_937799.1:n.-99A>G
NM_001354723.1:c.-99A>G NP_001341652.1:n.-99A>G
Search 100 bp 5'
Search 100 bp 3'