Canonical Allele Identifier: CA351748769

Gene: VHL

Linked Data

• ClinVar Variation Id: 1023005
• ClinVar RCV Id: RCV001322991
• dbSNP Id: rs1487408934
• MyVariant Identifiers: chr3:g.10183721C>A (hg19) ; chr3:g.10142037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142037C>A , CM000665.2:g.10142037C>A	GRCh38
NC_000003.11:g.10183721C>A , CM000665.1:g.10183721C>A	GRCh37
NC_000003.10:g.10158721C>A	NCBI36
NG_008212.3:g.5403C>A , LRG_322:g.5403C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.190C>A	ENSP00000512434.1:p.Arg64Ser
ENST00000696143.1:c.190C>A	ENSP00000512435.1:p.Arg64Ser
ENST00000696153.1:c.190C>A	ENSP00000512444.1:p.Arg64Ser
ENST00000256474.3:c.190C>A MANE Select	ENSP00000256474.3:p.Arg64Ser
ENST00000256474.2:c.190C>A	ENSP00000256474.2:p.Arg64Ser
ENST00000345392.2:c.190C>A	ENSP00000344757.2:p.Arg64Ser
NM_000551.3:c.190C>A , LRG_322t1:c.190C>A	NP_000542.1:p.Arg64Ser
NM_198156.2:c.190C>A	NP_937799.1:p.Arg64Ser
XM_011534078.1:c.190C>A	XP_011532380.1:p.Arg64Ser
NM_001354723.1:c.190C>A	NP_001341652.1:p.Arg64Ser
NM_000551.4:c.190C>A MANE Select	NP_000542.1:p.Arg64Ser
NM_001354723.2:c.190C>A	NP_001341652.1:p.Arg64Ser
NM_198156.3:c.190C>A	NP_937799.1:p.Arg64Ser