Canonical Allele Identifier: CA16042064
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 371897
dbSNP Id: rs778005138

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149972C>G , CM000665.2:g.10149972C>G GRCh38
NC_000003.11:g.10191656C>G , CM000665.1:g.10191656C>G GRCh37
NC_000003.10:g.10166656C>G NCBI36
NG_008212.3:g.13338C>G , LRG_322:g.13338C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*326C>G ENSP00000512434.1:n.*326C>G
ENST00000696143.1:c.785C>G ENSP00000512435.1:n.785C>G
ENST00000696153.1:c.*7C>G ENSP00000512444.1:n.*7C>G
ENST00000256474.3:c.*7C>G MANE Select ENSP00000256474.3:n.*7C>G
ENST00000256474.2:c.*7C>G ENSP00000256474.2:n.*7C>G
ENST00000345392.2:c.*7C>G ENSP00000344757.2:n.*7C>G
ENST00000477538.1:n.785C>G
NM_000551.3:c.*7C>G , LRG_322t1:c.*7C>G NP_000542.1:n.*7C>G
NM_198156.2:c.*7C>G NP_937799.1:n.*7C>G
NM_001354723.1:c.*203C>G NP_001341652.1:n.*203C>G
NM_000551.4:c.*7C>G MANE Select NP_000542.1:n.*7C>G
NM_001354723.2:c.*203C>G NP_001341652.1:n.*203C>G
NM_198156.3:c.*7C>G NP_937799.1:n.*7C>G