Canonical Allele Identifier: CA2664399404
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141462-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141462G>C , CM000665.2:g.10141462G>C GRCh38
NC_000003.11:g.10183146G>C , CM000665.1:g.10183146G>C GRCh37
NC_000003.10:g.10158146G>C NCBI36
NG_008212.3:g.4828G>C , LRG_322:g.4828G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-386G>C ENSP00000256474.2:n.-386G>C
Search 100 bp 5'
Search 100 bp 3'