Canonical Allele Identifier: CA2664399629
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141614-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141614T>C , CM000665.2:g.10141614T>C GRCh38
NC_000003.11:g.10183298T>C , CM000665.1:g.10183298T>C GRCh37
NC_000003.10:g.10158298T>C NCBI36
NG_008212.3:g.4980T>C , LRG_322:g.4980T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-234T>C ENSP00000256474.2:n.-234T>C
Search 100 bp 5'
Search 100 bp 3'