Canonical Allele Identifier: CA2664399666
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141636-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141636C>G , CM000665.2:g.10141636C>G GRCh38
NC_000003.11:g.10183320C>G , CM000665.1:g.10183320C>G GRCh37
NC_000003.10:g.10158320C>G NCBI36
NG_008212.3:g.5002C>G , LRG_322:g.5002C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-212C>G ENSP00000256474.2:n.-212C>G
NM_000551.3:c.-212C>G , LRG_322t1:c.-212C>G NP_000542.1:n.-212C>G
NM_198156.2:c.-212C>G NP_937799.1:n.-212C>G
NM_001354723.1:c.-212C>G NP_001341652.1:n.-212C>G
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