Canonical Allele Identifier: CA432536398

Gene: VHL

Linked Data

• ClinVar Variation Id: 526693
• ClinVar RCV Id: RCV000631296 ; RCV001013851
• dbSNP Id: rs1553619409
• COSMIC: COSM17705
• MyVariant Identifiers: chr3:g.10183726G>C (hg19) ; chr3:g.10142042G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142042G>C , CM000665.2:g.10142042G>C	GRCh38
NC_000003.11:g.10183726G>C , CM000665.1:g.10183726G>C	GRCh37
NC_000003.10:g.10158726G>C	NCBI36
NG_008212.3:g.5408G>C , LRG_322:g.5408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.195G>C	ENSP00000512434.1:p.Ser65=
ENST00000696143.1:c.195G>C	ENSP00000512435.1:p.Ser65=
ENST00000696153.1:c.195G>C	ENSP00000512444.1:p.Ser65=
ENST00000256474.3:c.195G>C MANE Select	ENSP00000256474.3:p.Ser65=
ENST00000256474.2:c.195G>C	ENSP00000256474.2:p.Ser65=
ENST00000345392.2:c.195G>C	ENSP00000344757.2:p.Ser65=
NM_000551.3:c.195G>C , LRG_322t1:c.195G>C	NP_000542.1:p.Ser65=
NM_198156.2:c.195G>C	NP_937799.1:p.Ser65=
XM_011534078.1:c.195G>C	XP_011532380.1:p.Ser65=
NM_001354723.1:c.195G>C	NP_001341652.1:p.Ser65=
NM_000551.4:c.195G>C MANE Select	NP_000542.1:p.Ser65=
NM_001354723.2:c.195G>C	NP_001341652.1:p.Ser65=
NM_198156.3:c.195G>C	NP_937799.1:p.Ser65=