Canonical Allele Identifier: CA291454147
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1053667950
gnomAD v2: 17-47440672-GACCCCAATAGC-G
gnomAD v3: 17-49363310-GACCCCAATAGC-G
gnomAD v4: 17-49363310-GACCCCAATAGC-G
MyVariant Identifiers: chr17:g.47440673_47440683del (hg19) chr17:g.49363311_49363321del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363313_49363323del , CM000679.2:g.49363313_49363323del GRCh38
NC_000017.10:g.47440675_47440685del , CM000679.1:g.47440675_47440685del GRCh37
NC_000017.9:g.44795674_44795684del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110882.1:n.136+796_136+806del
NR_110883.1:n.31-966_31-956del
NR_110884.1:n.58-966_58-956del
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