Canonical Allele Identifier: CA039449
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 215765
dbSNP Id: rs773519476
gnomAD v2: 3-10183666-G-A
gnomAD v3: 3-10141982-G-A
gnomAD v4: 3-10141982-G-A
COSMIC: COSM17998

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141982G>A , CM000665.2:g.10141982G>A GRCh38
NC_000003.11:g.10183666G>A , CM000665.1:g.10183666G>A GRCh37
NC_000003.10:g.10158666G>A NCBI36
NG_008212.3:g.5348G>A , LRG_322:g.5348G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.135G>A ENSP00000512434.1:p.Pro45=
ENST00000696143.1:c.135G>A ENSP00000512435.1:p.Pro45=
ENST00000696153.1:c.135G>A ENSP00000512444.1:p.Pro45=
ENST00000256474.3:c.135G>A MANE Select ENSP00000256474.3:p.Pro45=
ENST00000256474.2:c.135G>A ENSP00000256474.2:p.Pro45=
ENST00000345392.2:c.135G>A ENSP00000344757.2:p.Pro45=
NM_000551.3:c.135G>A , LRG_322t1:c.135G>A NP_000542.1:p.Pro45=
NM_198156.2:c.135G>A NP_937799.1:p.Pro45=
XM_011534078.1:c.135G>A XP_011532380.1:p.Pro45=
NM_001354723.1:c.135G>A NP_001341652.1:p.Pro45=
NM_000551.4:c.135G>A MANE Select NP_000542.1:p.Pro45=
NM_001354723.2:c.135G>A NP_001341652.1:p.Pro45=
NM_198156.3:c.135G>A NP_937799.1:p.Pro45=