Canonical Allele Identifier: CA626456590

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs1173241739
• gnomAD v2: 17-47440675-C-T
• gnomAD v3: 17-49363313-C-T
• gnomAD v4: 17-49363313-C-T
• MyVariant Identifiers: chr17:g.47440675C>T (hg19) ; chr17:g.49363313C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363313C>T , CM000679.2:g.49363313C>T	GRCh38
NC_000017.10:g.47440675C>T , CM000679.1:g.47440675C>T	GRCh37
NC_000017.9:g.44795674C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110882.1:n.136+796C>T
NR_110883.1:n.31-966C>T
NR_110884.1:n.58-966C>T