Canonical Allele Identifier: CA351750632
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs730882034
COSMIC: COSM14405
MyVariant Identifiers: chr3:g.10183788C>A (hg19) chr3:g.10142104C>A (hg38)
CIViC: CA351750632
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142104C>A , CM000665.2:g.10142104C>A GRCh38
NC_000003.11:g.10183788C>A , CM000665.1:g.10183788C>A GRCh37
NC_000003.10:g.10158788C>A NCBI36
NG_008212.3:g.5470C>A , LRG_322:g.5470C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.257C>A ENSP00000512434.1:p.Pro86His
ENST00000696143.1:c.257C>A ENSP00000512435.1:p.Pro86His
ENST00000696153.1:c.257C>A ENSP00000512444.1:p.Pro86His
ENST00000256474.3:c.257C>A MANE Select ENSP00000256474.3:p.Pro86His
ENST00000256474.2:c.257C>A ENSP00000256474.2:p.Pro86His
ENST00000345392.2:c.257C>A ENSP00000344757.2:p.Pro86His
NM_000551.3:c.257C>A , LRG_322t1:c.257C>A NP_000542.1:p.Pro86His
NM_198156.2:c.257C>A NP_937799.1:p.Pro86His
XM_011534078.1:c.257C>A XP_011532380.1:p.Pro86His
NM_001354723.1:c.257C>A NP_001341652.1:p.Pro86His
NM_000551.4:c.257C>A MANE Select NP_000542.1:p.Pro86His
NM_001354723.2:c.257C>A NP_001341652.1:p.Pro86His
NM_198156.3:c.257C>A NP_937799.1:p.Pro86His
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