Canonical Allele Identifier: CA351748610

Gene: VHL

Linked Data

• ClinVar Variation Id: 644898
• ClinVar RCV Id: RCV000798890 ; RCV001012789 ; RCV003467375
• dbSNP Id: rs1064795194
• gnomAD v4: 3-10142016-G-T
• MyVariant Identifiers: chr3:g.10183700G>T (hg19) ; chr3:g.10142016G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142016G>T , CM000665.2:g.10142016G>T	GRCh38
NC_000003.11:g.10183700G>T , CM000665.1:g.10183700G>T	GRCh37
NC_000003.10:g.10158700G>T	NCBI36
NG_008212.3:g.5382G>T , LRG_322:g.5382G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.169G>T	ENSP00000512434.1:p.Gly57Trp
ENST00000696143.1:c.169G>T	ENSP00000512435.1:p.Gly57Trp
ENST00000696153.1:c.169G>T	ENSP00000512444.1:p.Gly57Trp
ENST00000256474.3:c.169G>T MANE Select	ENSP00000256474.3:p.Gly57Trp
ENST00000256474.2:c.169G>T	ENSP00000256474.2:p.Gly57Trp
ENST00000345392.2:c.169G>T	ENSP00000344757.2:p.Gly57Trp
NM_000551.3:c.169G>T , LRG_322t1:c.169G>T	NP_000542.1:p.Gly57Trp
NM_198156.2:c.169G>T	NP_937799.1:p.Gly57Trp
XM_011534078.1:c.169G>T	XP_011532380.1:p.Gly57Trp
NM_001354723.1:c.169G>T	NP_001341652.1:p.Gly57Trp
NM_000551.4:c.169G>T MANE Select	NP_000542.1:p.Gly57Trp
NM_001354723.2:c.169G>T	NP_001341652.1:p.Gly57Trp
NM_198156.3:c.169G>T	NP_937799.1:p.Gly57Trp