Canonical Allele Identifier: CA291454016
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs576036948
gnomAD v2: 17-47440287-G-A
gnomAD v3: 17-49362925-G-A
gnomAD v4: 17-49362925-G-A
MyVariant Identifiers: chr17:g.47440287G>A (hg19) chr17:g.49362925G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49362925G>A , CM000679.2:g.49362925G>A GRCh38
NC_000017.10:g.47440287G>A , CM000679.1:g.47440287G>A GRCh37
NC_000017.9:g.44795286G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+408G>A
NR_110883.1:n.31-1354G>A
NR_110884.1:n.58-1354G>A
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