Canonical Allele Identifier: CA2664403066
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10152352-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152352G>T , CM000665.2:g.10152352G>T GRCh38
NC_000003.11:g.10194036G>T , CM000665.1:g.10194036G>T GRCh37
NC_000003.10:g.10169036G>T NCBI36
NG_008212.3:g.15718G>T , LRG_322:g.15718G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2387G>T ENSP00000512444.1:n.*2387G>T
ENST00000256474.3:c.*2387G>T MANE Select ENSP00000256474.3:n.*2387G>T
NM_000551.3:c.*2387G>T , LRG_322t1:c.*2387G>T NP_000542.1:n.*2387G>T
NM_198156.2:c.*2387G>T NP_937799.1:n.*2387G>T
NM_001354723.1:c.*2583G>T NP_001341652.1:n.*2583G>T
NM_000551.4:c.*2387G>T MANE Select NP_000542.1:n.*2387G>T
NM_001354723.2:c.*2583G>T NP_001341652.1:n.*2583G>T
NM_198156.3:c.*2387G>T NP_937799.1:n.*2387G>T
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