Canonical Allele Identifier: CA2577505213
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141756A>T , CM000665.2:g.10141756A>T GRCh38
NC_000003.11:g.10183440A>T , CM000665.1:g.10183440A>T GRCh37
NC_000003.10:g.10158440A>T NCBI36
NG_008212.3:g.5122A>T , LRG_322:g.5122A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-92A>T ENSP00000256474.2:n.-92A>T
NM_000551.3:c.-92A>T , LRG_322t1:c.-92A>T NP_000542.1:n.-92A>T
NM_198156.2:c.-92A>T NP_937799.1:n.-92A>T
NM_001354723.1:c.-92A>T NP_001341652.1:n.-92A>T