Canonical Allele Identifier: CA896157517
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1482426470
gnomAD v3: 3-10141711-C-T
gnomAD v4: 3-10141711-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141711C>T , CM000665.2:g.10141711C>T GRCh38
NC_000003.11:g.10183395C>T , CM000665.1:g.10183395C>T GRCh37
NC_000003.10:g.10158395C>T NCBI36
NG_008212.3:g.5077C>T , LRG_322:g.5077C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-137C>T ENSP00000256474.2:n.-137C>T
NM_000551.3:c.-137C>T , LRG_322t1:c.-137C>T NP_000542.1:n.-137C>T
NM_198156.2:c.-137C>T NP_937799.1:n.-137C>T
NM_001354723.1:c.-137C>T NP_001341652.1:n.-137C>T