Canonical Allele Identifier: CA2570341525
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10153146T>G , CM000665.2:g.10153146T>G GRCh38
NC_000003.11:g.10194830T>G , CM000665.1:g.10194830T>G GRCh37
NC_000003.10:g.10169830T>G NCBI36
NG_008212.3:g.16512T>G , LRG_322:g.16512T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*3181T>G ENSP00000512444.1:n.*3181T>G
ENST00000256474.3:c.*3181T>G MANE Select ENSP00000256474.3:n.*3181T>G
NM_000551.3:c.*3181T>G , LRG_322t1:c.*3181T>G NP_000542.1:n.*3181T>G
NM_198156.2:c.*3181T>G NP_937799.1:n.*3181T>G
NM_001354723.1:c.*3377T>G NP_001341652.1:n.*3377T>G
NM_000551.4:c.*3181T>G MANE Select NP_000542.1:n.*3181T>G
NM_001354723.2:c.*3377T>G NP_001341652.1:n.*3377T>G
NM_198156.3:c.*3181T>G NP_937799.1:n.*3181T>G