Canonical Allele Identifier: CA291454042
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs948896652
MyVariant Identifiers: chr17:g.49362969G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49362969G>A , CM000679.2:g.49362969G>A GRCh38
NC_000017.10:g.47440331G>A , CM000679.1:g.47440331G>A GRCh37
NC_000017.9:g.44795330G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+452G>A
NR_110883.1:n.31-1310G>A
NR_110884.1:n.58-1310G>A