Canonical Allele Identifier: CA2664403063
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10152349-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152349A>G , CM000665.2:g.10152349A>G GRCh38
NC_000003.11:g.10194033A>G , CM000665.1:g.10194033A>G GRCh37
NC_000003.10:g.10169033A>G NCBI36
NG_008212.3:g.15715A>G , LRG_322:g.15715A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2384A>G ENSP00000512444.1:n.*2384A>G
ENST00000256474.3:c.*2384A>G MANE Select ENSP00000256474.3:n.*2384A>G
NM_000551.3:c.*2384A>G , LRG_322t1:c.*2384A>G NP_000542.1:n.*2384A>G
NM_198156.2:c.*2384A>G NP_937799.1:n.*2384A>G
NM_001354723.1:c.*2580A>G NP_001341652.1:n.*2580A>G
NM_000551.4:c.*2384A>G MANE Select NP_000542.1:n.*2384A>G
NM_001354723.2:c.*2580A>G NP_001341652.1:n.*2580A>G
NM_198156.3:c.*2384A>G NP_937799.1:n.*2384A>G