Canonical Allele Identifier: CA2664399537
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141569-A-AAT
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141570_10141571insTA , CM000665.2:g.10141570_10141571insTA GRCh38
NC_000003.11:g.10183254_10183255insTA , CM000665.1:g.10183254_10183255insTA GRCh37
NC_000003.10:g.10158254_10158255insTA NCBI36
NG_008212.3:g.4936_4937insTA , LRG_322:g.4936_4937insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-278_-277insTA ENSP00000256474.2:n.-278_-277insTA
Search 100 bp 5'
Search 100 bp 3'