Canonical Allele Identifier: CA291454105

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs1005201895
• gnomAD v3: 17-49363181-G-T
• gnomAD v4: 17-49363181-G-T
• MyVariant Identifiers: chr17:g.47440543G>T (hg19) ; chr17:g.49363181G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363181G>T , CM000679.2:g.49363181G>T	GRCh38
NC_000017.10:g.47440543G>T , CM000679.1:g.47440543G>T	GRCh37
NC_000017.9:g.44795542G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+664G>T
NR_110883.1:n.31-1098G>T
NR_110884.1:n.58-1098G>T