Canonical Allele Identifier: CA984408281
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1567705939
gnomAD v3: 17-49362903-G-T
gnomAD v4: 17-49362903-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49362903G>T , CM000679.2:g.49362903G>T GRCh38
NC_000017.10:g.47440265G>T , CM000679.1:g.47440265G>T GRCh37
NC_000017.9:g.44795264G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+386G>T
NR_110883.1:n.31-1376G>T
NR_110884.1:n.58-1376G>T
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