Canonical Allele Identifier: CA2702129695

Gene: VHL

Linked Data

• dbSNP Id: rs2125123901

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141442_10141448del , CM000665.2:g.10141442_10141448del	GRCh38
NC_000003.11:g.10183126_10183132del , CM000665.1:g.10183126_10183132del	GRCh37
NC_000003.10:g.10158126_10158132del	NCBI36
NG_008212.3:g.4808_4814del , LRG_322:g.4808_4814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256474.2:c.-406_-400del	ENSP00000256474.2:n.-406_-400del