Canonical Allele Identifier: CA351756627

Gene: VHL

Linked Data

• dbSNP Id: rs2125130811
• MyVariant Identifiers: chr3:g.10191616G>T (hg19) ; chr3:g.10149932G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149932G>T , CM000665.2:g.10149932G>T	GRCh38
NC_000003.11:g.10191616G>T , CM000665.1:g.10191616G>T	GRCh37
NC_000003.10:g.10166616G>T	NCBI36
NG_008212.3:g.13298G>T , LRG_322:g.13298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*286G>T	ENSP00000512434.1:n.*286G>T
ENST00000696143.1:c.745G>T	ENSP00000512435.1:n.745G>T
ENST00000696153.1:c.720G>T	ENSP00000512444.1:p.Gln240His
ENST00000256474.3:c.609G>T MANE Select	ENSP00000256474.3:p.Gln203His
ENST00000256474.2:c.609G>T	ENSP00000256474.2:p.Gln203His
ENST00000345392.2:c.486G>T	ENSP00000344757.2:p.Gln162His
ENST00000477538.1:n.745G>T
NM_000551.3:c.609G>T , LRG_322t1:c.609G>T	NP_000542.1:p.Gln203His
NM_198156.2:c.486G>T	NP_937799.1:p.Gln162His
NM_001354723.1:c.*163G>T	NP_001341652.1:n.*163G>T
NM_000551.4:c.609G>T MANE Select	NP_000542.1:p.Gln203His
NM_001354723.2:c.*163G>T	NP_001341652.1:n.*163G>T
NM_198156.3:c.486G>T	NP_937799.1:p.Gln162His