Canonical Allele Identifier: CA626456597
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1335360701
gnomAD v2: 17-47440690-ACATTTT-A
gnomAD v3: 17-49363328-ACATTTT-A
gnomAD v4: 17-49363328-ACATTTT-A
MyVariant Identifiers: chr17:g.47440691_47440696del (hg19) chr17:g.49363329_49363334del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363330_49363335del , CM000679.2:g.49363330_49363335del GRCh38
NC_000017.10:g.47440692_47440697del , CM000679.1:g.47440692_47440697del GRCh37
NC_000017.9:g.44795691_44795696del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110882.1:n.136+813_136+818del
NR_110883.1:n.31-949_31-944del
NR_110884.1:n.58-949_58-944del
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