Canonical Allele Identifier: CA1345065371
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1696441190
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152596G>A , CM000665.2:g.10152596G>A GRCh38
NC_000003.11:g.10194280G>A , CM000665.1:g.10194280G>A GRCh37
NC_000003.10:g.10169280G>A NCBI36
NG_008212.3:g.15962G>A , LRG_322:g.15962G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2631G>A ENSP00000512444.1:n.*2631G>A
ENST00000256474.3:c.*2631G>A MANE Select ENSP00000256474.3:n.*2631G>A
NM_000551.3:c.*2631G>A , LRG_322t1:c.*2631G>A NP_000542.1:n.*2631G>A
NM_198156.2:c.*2631G>A NP_937799.1:n.*2631G>A
NM_001354723.1:c.*2827G>A NP_001341652.1:n.*2827G>A
NM_000551.4:c.*2631G>A MANE Select NP_000542.1:n.*2631G>A
NM_001354723.2:c.*2827G>A NP_001341652.1:n.*2827G>A
NM_198156.3:c.*2631G>A NP_937799.1:n.*2631G>A
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