Canonical Allele Identifier: CA291454101

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs375317564
• gnomAD v2: 17-47440491-G-C
• gnomAD v3: 17-49363129-G-C
• gnomAD v4: 17-49363129-G-C
• MyVariant Identifiers: chr17:g.47440491G>C (hg19) ; chr17:g.49363129G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363129G>C , CM000679.2:g.49363129G>C	GRCh38
NC_000017.10:g.47440491G>C , CM000679.1:g.47440491G>C	GRCh37
NC_000017.9:g.44795490G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110882.1:n.136+612G>C
NR_110883.1:n.31-1150G>C
NR_110884.1:n.58-1150G>C