Canonical Allele Identifier: CA1345064395
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141728C= , CM000665.2:g.10141728C= GRCh38
NC_000003.11:g.10183412C= , CM000665.1:g.10183412C= GRCh37
NC_000003.10:g.10158412C= NCBI36
NG_008212.3:g.5094C= , LRG_322:g.5094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-120C= ENSP00000256474.2:n.-120C=
NM_000551.3:c.-120C= , LRG_322t1:c.-120C= NP_000542.1:n.-120C=
NM_198156.2:c.-120C= NP_937799.1:n.-120C=
NM_001354723.1:c.-120C= NP_001341652.1:n.-120C=