Canonical Allele Identifier: CA896168010
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1173072996
MyVariant Identifiers: chr3:g.10194369del (hg19) chr3:g.10152685del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152687del , CM000665.2:g.10152687del GRCh38
NC_000003.11:g.10194371del , CM000665.1:g.10194371del GRCh37
NC_000003.10:g.10169371del NCBI36
NG_008212.3:g.16053del , LRG_322:g.16053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2722del ENSP00000512444.1:n.*2722del
ENST00000256474.3:c.*2722del MANE Select ENSP00000256474.3:n.*2722del
NM_000551.3:c.*2722del , LRG_322t1:c.*2722del NP_000542.1:n.*2722del
NM_198156.2:c.*2722del NP_937799.1:n.*2722del
NM_001354723.1:c.*2918del NP_001341652.1:n.*2918del
NM_000551.4:c.*2722del MANE Select NP_000542.1:n.*2722del
NM_001354723.2:c.*2918del NP_001341652.1:n.*2918del
NM_198156.3:c.*2722del NP_937799.1:n.*2722del
Search 100 bp 5'
Search 100 bp 3'