ClinGen Allele Registry
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Canonical Allele Identifier:
CA316149265
Gene: ZNF217-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs972540732
gnomAD v3:
20-53566940-T-C
gnomAD v4:
20-53566940-T-C
MyVariant Identifiers:
chr20:g.52183479T>C (hg19)
chr20:g.53566940T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.53566940T>C , CM000682.2:g.53566940T>C
GRCh38
NC_000020.10:g.52183479T>C , CM000682.1:g.52183479T>C
GRCh37
NC_000020.9:g.51616886T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110051.1:n.556-3332T>C
Search 100 bp 5'
Search 100 bp 3'