Canonical Allele Identifier: CA2664399540
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141570-A-AAT
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141571_10141572insTA , CM000665.2:g.10141571_10141572insTA GRCh38
NC_000003.11:g.10183255_10183256insTA , CM000665.1:g.10183255_10183256insTA GRCh37
NC_000003.10:g.10158255_10158256insTA NCBI36
NG_008212.3:g.4937_4938insTA , LRG_322:g.4937_4938insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-277_-276insTA ENSP00000256474.2:n.-277_-276insTA
Search 100 bp 5'
Search 100 bp 3'