Canonical Allele Identifier: CA357036
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223164
dbSNP Id: rs869025619
gnomAD v4: 3-10142064-C-T
COSMIC: COSM17872
CIViC: CA357036

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142064C>T , CM000665.2:g.10142064C>T GRCh38
NC_000003.11:g.10183748C>T , CM000665.1:g.10183748C>T GRCh37
NC_000003.10:g.10158748C>T NCBI36
NG_008212.3:g.5430C>T , LRG_322:g.5430C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.217C>T ENSP00000512434.1:p.Gln73Ter
ENST00000696143.1:c.217C>T ENSP00000512435.1:p.Gln73Ter
ENST00000696153.1:c.217C>T ENSP00000512444.1:p.Gln73Ter
ENST00000256474.3:c.217C>T MANE Select ENSP00000256474.3:p.Gln73Ter
ENST00000256474.2:c.217C>T ENSP00000256474.2:p.Gln73Ter
ENST00000345392.2:c.217C>T ENSP00000344757.2:p.Gln73Ter
NM_000551.3:c.217C>T , LRG_322t1:c.217C>T NP_000542.1:p.Gln73Ter
NM_198156.2:c.217C>T NP_937799.1:p.Gln73Ter
XM_011534078.1:c.217C>T XP_011532380.1:p.Gln73Ter
NM_001354723.1:c.217C>T NP_001341652.1:p.Gln73Ter
NM_000551.4:c.217C>T MANE Select NP_000542.1:p.Gln73Ter
NM_001354723.2:c.217C>T NP_001341652.1:p.Gln73Ter
NM_198156.3:c.217C>T NP_937799.1:p.Gln73Ter