Canonical Allele Identifier: CA540875324
Gene: VHL HGNC NCBI

Linked Data

gnomAD v2: 3-10183234-C-A
gnomAD v3: 3-10141550-C-A
gnomAD v4: 3-10141550-C-A
MyVariant Identifiers: chr3:g.10183234C>A (hg19) chr3:g.10141550C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141550C>A , CM000665.2:g.10141550C>A GRCh38
NC_000003.11:g.10183234C>A , CM000665.1:g.10183234C>A GRCh37
NC_000003.10:g.10158234C>A NCBI36
NG_008212.3:g.4916C>A , LRG_322:g.4916C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-298C>A ENSP00000256474.2:n.-298C>A
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