Canonical Allele Identifier: CA2664399485
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141537-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141537G>T , CM000665.2:g.10141537G>T GRCh38
NC_000003.11:g.10183221G>T , CM000665.1:g.10183221G>T GRCh37
NC_000003.10:g.10158221G>T NCBI36
NG_008212.3:g.4903G>T , LRG_322:g.4903G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-311G>T ENSP00000256474.2:n.-311G>T
Search 100 bp 5'
Search 100 bp 3'