Canonical Allele Identifier: CA896157366

Gene: VHL

Linked Data

• dbSNP Id: rs1329789661
• MyVariant Identifiers: chr3:g.10183324_10183327del (hg19) ; chr3:g.10141640_10141643del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141641_10141644del , CM000665.2:g.10141641_10141644del	GRCh38
NC_000003.11:g.10183325_10183328del , CM000665.1:g.10183325_10183328del	GRCh37
NC_000003.10:g.10158325_10158328del	NCBI36
NG_008212.3:g.5007_5010del , LRG_322:g.5007_5010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256474.2:c.-207_-204del	ENSP00000256474.2:n.-207_-204del
NM_000551.3:c.-207_-204del , LRG_322t1:c.-207_-204del	NP_000542.1:n.-207_-204del
NM_198156.2:c.-207_-204del	NP_937799.1:n.-207_-204del
NM_001354723.1:c.-207_-204del	NP_001341652.1:n.-207_-204del