Canonical Allele Identifier: CA984408298
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2070422141
gnomAD v3: 17-49363250-T-C
gnomAD v4: 17-49363250-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363250T>C , CM000679.2:g.49363250T>C GRCh38
NC_000017.10:g.47440612T>C , CM000679.1:g.47440612T>C GRCh37
NC_000017.9:g.44795611T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+733T>C
NR_110883.1:n.31-1029T>C
NR_110884.1:n.58-1029T>C
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