ClinGen Allele Registry
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Canonical Allele Identifier:
CA316149238
Gene: ZNF217-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs902864981
MyVariant Identifiers:
chr20:g.52183437G>C (hg19)
chr20:g.53566898G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.53566898G>C , CM000682.2:g.53566898G>C
GRCh38
NC_000020.10:g.52183437G>C , CM000682.1:g.52183437G>C
GRCh37
NC_000020.9:g.51616844G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110051.1:n.556-3374G>C
Search 100 bp 5'
Search 100 bp 3'