Canonical Allele Identifier: CA896168495

Gene: VHL

Linked Data

• dbSNP Id: rs1387016130
• MyVariant Identifiers: chr3:g.10194986T>G (hg19) ; chr3:g.10153302T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10153302T>G , CM000665.2:g.10153302T>G	GRCh38
NC_000003.11:g.10194986T>G , CM000665.1:g.10194986T>G	GRCh37
NC_000003.10:g.10169986T>G	NCBI36
NG_008212.3:g.16668T>G , LRG_322:g.16668T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696153.1:c.*3337T>G	ENSP00000512444.1:n.*3337T>G
ENST00000256474.3:c.*3337T>G MANE Select	ENSP00000256474.3:n.*3337T>G
NM_000551.3:c.*3337T>G , LRG_322t1:c.*3337T>G	NP_000542.1:n.*3337T>G
NM_198156.2:c.*3337T>G	NP_937799.1:n.*3337T>G
NM_001354723.1:c.*3533T>G	NP_001341652.1:n.*3533T>G
NM_000551.4:c.*3337T>G MANE Select	NP_000542.1:n.*3337T>G
NM_001354723.2:c.*3533T>G	NP_001341652.1:n.*3533T>G
NM_198156.3:c.*3337T>G	NP_937799.1:n.*3337T>G