Canonical Allele Identifier: CA291454021
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1049619594
gnomAD v2: 17-47440293-A-G
gnomAD v3: 17-49362931-A-G
gnomAD v4: 17-49362931-A-G
MyVariant Identifiers: chr17:g.47440293A>G (hg19) chr17:g.49362931A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49362931A>G , CM000679.2:g.49362931A>G GRCh38
NC_000017.10:g.47440293A>G , CM000679.1:g.47440293A>G GRCh37
NC_000017.9:g.44795292A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110882.1:n.136+414A>G
NR_110883.1:n.31-1348A>G
NR_110884.1:n.58-1348A>G
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