Canonical Allele Identifier: CA540877377

Gene: VHL

Linked Data

• dbSNP Id: rs376485698
• gnomAD v2: 3-10192722-G-A
• gnomAD v4: 3-10151038-G-A
• MyVariant Identifiers: chr3:g.10192722G>A (hg19) ; chr3:g.10151038G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151038G>A , CM000665.2:g.10151038G>A	GRCh38
NC_000003.11:g.10192722G>A , CM000665.1:g.10192722G>A	GRCh37
NC_000003.10:g.10167722G>A	NCBI36
NG_008212.3:g.14404G>A , LRG_322:g.14404G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*1392G>A	ENSP00000512434.1:n.*1392G>A
ENST00000696143.1:c.1851G>A	ENSP00000512435.1:n.1851G>A
ENST00000696153.1:c.*1073G>A	ENSP00000512444.1:n.*1073G>A
ENST00000256474.3:c.*1073G>A MANE Select	ENSP00000256474.3:n.*1073G>A
ENST00000256474.2:c.*1073G>A	ENSP00000256474.2:n.*1073G>A
ENST00000345392.2:c.*1073G>A	ENSP00000344757.2:n.*1073G>A
NM_000551.3:c.*1073G>A , LRG_322t1:c.*1073G>A	NP_000542.1:n.*1073G>A
NM_198156.2:c.*1073G>A	NP_937799.1:n.*1073G>A
NM_001354723.1:c.*1269G>A	NP_001341652.1:n.*1269G>A
NM_000551.4:c.*1073G>A MANE Select	NP_000542.1:n.*1073G>A
NM_001354723.2:c.*1269G>A	NP_001341652.1:n.*1269G>A
NM_198156.3:c.*1073G>A	NP_937799.1:n.*1073G>A