Canonical Allele Identifier: CA351747567

Gene: VHL

Linked Data

• ClinVar Variation Id: 945878
• ClinVar RCV Id: RCV001216618
• dbSNP Id: rs913104799
• gnomAD v4: 3-10141935-G-T
• MyVariant Identifiers: chr3:g.10183619G>T (hg19) ; chr3:g.10141935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141935G>T , CM000665.2:g.10141935G>T	GRCh38
NC_000003.11:g.10183619G>T , CM000665.1:g.10183619G>T	GRCh37
NC_000003.10:g.10158619G>T	NCBI36
NG_008212.3:g.5301G>T , LRG_322:g.5301G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.88G>T	ENSP00000512434.1:p.Gly30Trp
ENST00000696143.1:c.88G>T	ENSP00000512435.1:p.Gly30Trp
ENST00000696153.1:c.88G>T	ENSP00000512444.1:p.Gly30Trp
ENST00000256474.3:c.88G>T MANE Select	ENSP00000256474.3:p.Gly30Trp
ENST00000256474.2:c.88G>T	ENSP00000256474.2:p.Gly30Trp
ENST00000345392.2:c.88G>T	ENSP00000344757.2:p.Gly30Trp
NM_000551.3:c.88G>T , LRG_322t1:c.88G>T	NP_000542.1:p.Gly30Trp
NM_198156.2:c.88G>T	NP_937799.1:p.Gly30Trp
XM_011534078.1:c.88G>T	XP_011532380.1:p.Gly30Trp
NM_001354723.1:c.88G>T	NP_001341652.1:p.Gly30Trp
NM_000551.4:c.88G>T MANE Select	NP_000542.1:p.Gly30Trp
NM_001354723.2:c.88G>T	NP_001341652.1:p.Gly30Trp
NM_198156.3:c.88G>T	NP_937799.1:p.Gly30Trp