Canonical Allele Identifier: CA772723367

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs1329753204
• gnomAD v3: 17-49363159-G-C
• gnomAD v4: 17-49363159-G-C
• MyVariant Identifiers: chr17:g.47440521G>C (hg19) ; chr17:g.49363159G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363159G>C , CM000679.2:g.49363159G>C	GRCh38
NC_000017.10:g.47440521G>C , CM000679.1:g.47440521G>C	GRCh37
NC_000017.9:g.44795520G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+642G>C
NR_110883.1:n.31-1120G>C
NR_110884.1:n.58-1120G>C