Canonical Allele Identifier: CA1345064227
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141633_10141653delinsAGCCTCGCCTCCGTTACAACG , CM000665.2:g.10141633_10141653delinsAGCCTCGCCTCCGTTACAACG GRCh38
NC_000003.11:g.10183317_10183337delinsAGCCTCGCCTCCGTTACAACG , CM000665.1:g.10183317_10183337delinsAGCCTCGCCTCCGTTACAACG GRCh37
NC_000003.10:g.10158317_10158337delinsAGCCTCGCCTCCGTTACAACG NCBI36
NG_008212.3:g.4999_5019delinsAGCCTCGCCTCCGTTACAACG , LRG_322:g.4999_5019delinsAGCCTCGCCTCCGTTACAACG

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-215_-195delinsAGCCTCGCCTCCGTTACAACG ENSP00000256474.2:n.-215_-195delinsAGCCTCGCCTCCGTTACAACG