Canonical Allele Identifier: CA351756116
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1553620313

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149807T>G , CM000665.2:g.10149807T>G GRCh38
NC_000003.11:g.10191491T>G , CM000665.1:g.10191491T>G GRCh37
NC_000003.10:g.10166491T>G NCBI36
NG_008212.3:g.13173T>G , LRG_322:g.13173T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*161T>G ENSP00000512434.1:n.*161T>G
ENST00000696143.1:c.620T>G ENSP00000512435.1:n.620T>G
ENST00000696153.1:c.595T>G ENSP00000512444.1:p.Cys199Gly
ENST00000256474.3:c.484T>G MANE Select ENSP00000256474.3:p.Cys162Gly
ENST00000256474.2:c.484T>G ENSP00000256474.2:p.Cys162Gly
ENST00000345392.2:c.361T>G ENSP00000344757.2:p.Cys121Gly
ENST00000477538.1:n.620T>G
NM_000551.3:c.484T>G , LRG_322t1:c.484T>G NP_000542.1:p.Cys162Gly
NM_198156.2:c.361T>G NP_937799.1:p.Cys121Gly
NM_001354723.1:c.*38T>G NP_001341652.1:n.*38T>G
NM_000551.4:c.484T>G MANE Select NP_000542.1:p.Cys162Gly
NM_001354723.2:c.*38T>G NP_001341652.1:n.*38T>G
NM_198156.3:c.361T>G NP_937799.1:p.Cys121Gly