Canonical Allele Identifier: CA772723457
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1359076341
MyVariant Identifiers: chr17:g.47440662del (hg19) chr17:g.49363300del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363300del , CM000679.2:g.49363300del GRCh38
NC_000017.10:g.47440662del , CM000679.1:g.47440662del GRCh37
NC_000017.9:g.44795661del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110882.1:n.136+783del
NR_110883.1:n.31-979del
NR_110884.1:n.58-979del
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