Canonical Allele Identifier: CA1345064237
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141639G= , CM000665.2:g.10141639G= GRCh38
NC_000003.11:g.10183323G= , CM000665.1:g.10183323G= GRCh37
NC_000003.10:g.10158323G= NCBI36
NG_008212.3:g.5005G= , LRG_322:g.5005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-209G= ENSP00000256474.2:n.-209G=
NM_000551.3:c.-209G= , LRG_322t1:c.-209G= NP_000542.1:n.-209G=
NM_198156.2:c.-209G= NP_937799.1:n.-209G=
NM_001354723.1:c.-209G= NP_001341652.1:n.-209G=