Canonical Allele Identifier: CA351751321
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 633016
ClinVar RCV Id: RCV001039507
dbSNP Id: rs1559426203
gnomAD v4: 3-10142178-A-G
COSMIC: COSM18353

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142178A>G , CM000665.2:g.10142178A>G GRCh38
NC_000003.11:g.10183862A>G , CM000665.1:g.10183862A>G GRCh37
NC_000003.10:g.10158862A>G NCBI36
NG_008212.3:g.5544A>G , LRG_322:g.5544A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.331A>G ENSP00000512434.1:p.Ser111Gly
ENST00000696143.1:c.331A>G ENSP00000512435.1:p.Ser111Gly
ENST00000696153.1:c.331A>G ENSP00000512444.1:p.Ser111Gly
ENST00000256474.3:c.331A>G MANE Select ENSP00000256474.3:p.Ser111Gly
ENST00000256474.2:c.331A>G ENSP00000256474.2:p.Ser111Gly
ENST00000345392.2:c.331A>G ENSP00000344757.2:p.Ser111Gly
NM_000551.3:c.331A>G , LRG_322t1:c.331A>G NP_000542.1:p.Ser111Gly
NM_198156.2:c.331A>G NP_937799.1:p.Ser111Gly
XM_011534078.1:c.331A>G XP_011532380.1:p.Ser111Gly
NM_001354723.1:c.331A>G NP_001341652.1:p.Ser111Gly
NM_000551.4:c.331A>G MANE Select NP_000542.1:p.Ser111Gly
NM_001354723.2:c.331A>G NP_001341652.1:p.Ser111Gly
NM_198156.3:c.331A>G NP_937799.1:p.Ser111Gly