Canonical Allele Identifier: CA896157307
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1210283059
MyVariant Identifiers: chr3:g.10183252_10183253insAC (hg19) chr3:g.10141568_10141569insAC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141569_10141570insCA , CM000665.2:g.10141569_10141570insCA GRCh38
NC_000003.11:g.10183253_10183254insCA , CM000665.1:g.10183253_10183254insCA GRCh37
NC_000003.10:g.10158253_10158254insCA NCBI36
NG_008212.3:g.4935_4936insCA , LRG_322:g.4935_4936insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256474.2:c.-279_-278insCA ENSP00000256474.2:n.-279_-278insCA
Search 100 bp 5'
Search 100 bp 3'