Canonical Allele Identifier: CA316149233
Gene: ZNF217-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1009132170
gnomAD v3: 20-53566886-C-T
gnomAD v4: 20-53566886-C-T
MyVariant Identifiers: chr20:g.52183425C>T (hg19) chr20:g.53566886C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53566886C>T , CM000682.2:g.53566886C>T GRCh38
NC_000020.10:g.52183425C>T , CM000682.1:g.52183425C>T GRCh37
NC_000020.9:g.51616832C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110051.1:n.556-3386C>T
Search 100 bp 5'
Search 100 bp 3'