Canonical Allele Identifier: CA626456452

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs1358107994
• gnomAD v2: 17-47440467-T-C
• gnomAD v3: 17-49363105-T-C
• gnomAD v4: 17-49363105-T-C
• COSMIC: COSN7437245
• MyVariant Identifiers: chr17:g.47440467T>C (hg19) ; chr17:g.49363105T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363105T>C , CM000679.2:g.49363105T>C	GRCh38
NC_000017.10:g.47440467T>C , CM000679.1:g.47440467T>C	GRCh37
NC_000017.9:g.44795466T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+588T>C
NR_110883.1:n.31-1174T>C
NR_110884.1:n.58-1174T>C