Canonical Allele Identifier: CA541213572

Gene: VHL

Linked Data

• dbSNP Id: rs1349160967
• gnomAD v2: 3-10188357-T-C
• gnomAD v3: 3-10146673-T-C
• gnomAD v4: 3-10146673-T-C
• MyVariant Identifiers: chr3:g.10188357T>C (hg19) ; chr3:g.10146673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146673T>C , CM000665.2:g.10146673T>C	GRCh38
NC_000003.11:g.10188357T>C , CM000665.1:g.10188357T>C	GRCh37
NC_000003.10:g.10163357T>C	NCBI36
NG_008212.3:g.10039T>C , LRG_322:g.10039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*140+37T>C	ENSP00000512434.1:n.*140+37T>C
ENST00000696143.1:c.600-3114T>C	ENSP00000512435.1:n.600-3114T>C
ENST00000696153.1:c.463+37T>C	ENSP00000512444.1:n.463+37T>C
ENST00000256474.3:c.463+37T>C MANE Select	ENSP00000256474.3:n.463+37T>C
ENST00000256474.2:c.463+37T>C	ENSP00000256474.2:n.463+37T>C
ENST00000345392.2:c.341-3114T>C	ENSP00000344757.2:n.341-3114T>C
ENST00000477538.1:n.599+37T>C
NM_000551.3:c.463+37T>C , LRG_322t1:c.463+37T>C	NP_000542.1:n.463+37T>C
NM_198156.2:c.341-3114T>C	NP_937799.1:n.341-3114T>C
NM_001354723.1:c.*18-3114T>C	NP_001341652.1:n.*18-3114T>C
NM_000551.4:c.463+37T>C MANE Select	NP_000542.1:n.463+37T>C
NM_001354723.2:c.*18-3114T>C	NP_001341652.1:n.*18-3114T>C
NM_198156.3:c.341-3114T>C	NP_937799.1:n.341-3114T>C