Canonical Allele Identifier: CA1345064368
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141707T= , CM000665.2:g.10141707T= GRCh38
NC_000003.11:g.10183391T= , CM000665.1:g.10183391T= GRCh37
NC_000003.10:g.10158391T= NCBI36
NG_008212.3:g.5073T= , LRG_322:g.5073T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-141T= ENSP00000256474.2:n.-141T=
NM_000551.3:c.-141T= , LRG_322t1:c.-141T= NP_000542.1:n.-141T=
NM_198156.2:c.-141T= NP_937799.1:n.-141T=
NM_001354723.1:c.-141T= NP_001341652.1:n.-141T=