ClinGen Allele Registry
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Canonical Allele Identifier:
CA635815832
Gene: ZNF217-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1268525508
gnomAD v2:
20-52183426-G-A
gnomAD v3:
20-53566887-G-A
gnomAD v4:
20-53566887-G-A
MyVariant Identifiers:
chr20:g.52183426G>A (hg19)
chr20:g.53566887G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.53566887G>A , CM000682.2:g.53566887G>A
GRCh38
NC_000020.10:g.52183426G>A , CM000682.1:g.52183426G>A
GRCh37
NC_000020.9:g.51616833G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110051.1:n.556-3385G>A
Search 100 bp 5'
Search 100 bp 3'