Canonical Allele Identifier: CA291454071

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs999083849
• gnomAD v2: 17-47440435-A-C
• gnomAD v3: 17-49363073-A-C
• gnomAD v4: 17-49363073-A-C
• MyVariant Identifiers: chr17:g.47440435A>C (hg19) ; chr17:g.49363073A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363073A>C , CM000679.2:g.49363073A>C	GRCh38
NC_000017.10:g.47440435A>C , CM000679.1:g.47440435A>C	GRCh37
NC_000017.9:g.44795434A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+556A>C
NR_110883.1:n.31-1206A>C
NR_110884.1:n.58-1206A>C