Canonical Allele Identifier: CA2664399659

Gene: VHL

Linked Data

• gnomAD v4: 3-10141633-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141633A>C , CM000665.2:g.10141633A>C	GRCh38
NC_000003.11:g.10183317A>C , CM000665.1:g.10183317A>C	GRCh37
NC_000003.10:g.10158317A>C	NCBI36
NG_008212.3:g.4999A>C , LRG_322:g.4999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256474.2:c.-215A>C	ENSP00000256474.2:n.-215A>C