Canonical Allele Identifier: CA14380335

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs16948048
• gnomAD v2: 17-47440466-A-G
• gnomAD v3: 17-49363104-A-G
• gnomAD v4: 17-49363104-A-G
• MyVariant Identifiers: chr17:g.47440466A>G (hg19) ; chr17:g.49363104A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363104A>G , CM000679.2:g.49363104A>G	GRCh38
NC_000017.10:g.47440466A>G , CM000679.1:g.47440466A>G	GRCh37
NC_000017.9:g.44795465A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+587A>G
NR_110883.1:n.31-1175A>G
NR_110884.1:n.58-1175A>G