Canonical Allele Identifier: CA772723389
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1455347043
MyVariant Identifiers: chr17:g.47440551G>A (hg19) chr17:g.49363189G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363189G>A , CM000679.2:g.49363189G>A GRCh38
NC_000017.10:g.47440551G>A , CM000679.1:g.47440551G>A GRCh37
NC_000017.9:g.44795550G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+672G>A
NR_110883.1:n.31-1090G>A
NR_110884.1:n.58-1090G>A
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