Canonical Allele Identifier: CA1345064381
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141719C= , CM000665.2:g.10141719C= GRCh38
NC_000003.11:g.10183403C= , CM000665.1:g.10183403C= GRCh37
NC_000003.10:g.10158403C= NCBI36
NG_008212.3:g.5085C= , LRG_322:g.5085C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-129C= ENSP00000256474.2:n.-129C=
NM_000551.3:c.-129C= , LRG_322t1:c.-129C= NP_000542.1:n.-129C=
NM_198156.2:c.-129C= NP_937799.1:n.-129C=
NM_001354723.1:c.-129C= NP_001341652.1:n.-129C=