Canonical Allele Identifier: CA541213497

Gene: VHL

Linked Data

• ClinVar Variation Id: 508543
• ClinVar RCV Id: RCV000613667 ; RCV003962757
• dbSNP Id: rs1340337531
• gnomAD v2: 3-10183507-C-A
• gnomAD v3: 3-10141823-C-A
• gnomAD v4: 3-10141823-C-A
• MyVariant Identifiers: chr3:g.10183507C>A (hg19) ; chr3:g.10141823C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141823C>A , CM000665.2:g.10141823C>A	GRCh38
NC_000003.11:g.10183507C>A , CM000665.1:g.10183507C>A	GRCh37
NC_000003.10:g.10158507C>A	NCBI36
NG_008212.3:g.5189C>A , LRG_322:g.5189C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.-25C>A	ENSP00000512434.1:n.-25C>A
ENST00000696153.1:c.-25C>A	ENSP00000512444.1:n.-25C>A
ENST00000256474.3:c.-25C>A MANE Select	ENSP00000256474.3:n.-25C>A
ENST00000256474.2:c.-25C>A	ENSP00000256474.2:n.-25C>A
ENST00000345392.2:c.-25C>A	ENSP00000344757.2:n.-25C>A
NM_000551.3:c.-25C>A , LRG_322t1:c.-25C>A	NP_000542.1:n.-25C>A
NM_198156.2:c.-25C>A	NP_937799.1:n.-25C>A
XM_011534078.1:c.-25C>A	XP_011532380.1:n.-25C>A
NM_001354723.1:c.-25C>A	NP_001341652.1:n.-25C>A
NM_000551.4:c.-25C>A MANE Select	NP_000542.1:n.-25C>A
NM_001354723.2:c.-25C>A	NP_001341652.1:n.-25C>A
NM_198156.3:c.-25C>A	NP_937799.1:n.-25C>A