Canonical Allele Identifier: CA1345064292
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141661G= , CM000665.2:g.10141661G= GRCh38
NC_000003.11:g.10183345G= , CM000665.1:g.10183345G= GRCh37
NC_000003.10:g.10158345G= NCBI36
NG_008212.3:g.5027G= , LRG_322:g.5027G=

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-187G= ENSP00000256474.2:n.-187G=
NM_000551.3:c.-187G= , LRG_322t1:c.-187G= NP_000542.1:n.-187G=
NM_198156.2:c.-187G= NP_937799.1:n.-187G=
NM_001354723.1:c.-187G= NP_001341652.1:n.-187G=