Canonical Allele Identifier: CA772723245
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1242231917
gnomAD v3: 17-49362912-C-G
gnomAD v4: 17-49362912-C-G
MyVariant Identifiers: chr17:g.47440274C>G (hg19) chr17:g.49362912C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49362912C>G , CM000679.2:g.49362912C>G GRCh38
NC_000017.10:g.47440274C>G , CM000679.1:g.47440274C>G GRCh37
NC_000017.9:g.44795273C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+395C>G
NR_110883.1:n.31-1367C>G
NR_110884.1:n.58-1367C>G
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