Canonical Allele Identifier: CA316149385
Gene: ZNF217-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs75839044
gnomAD v2: 20-52183600-A-T
gnomAD v3: 20-53567061-A-T
gnomAD v4: 20-53567061-A-T
MyVariant Identifiers: chr20:g.52183600A>T (hg19) chr20:g.53567061A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53567061A>T , CM000682.2:g.53567061A>T GRCh38
NC_000020.10:g.52183600A>T , CM000682.1:g.52183600A>T GRCh37
NC_000020.9:g.51617007A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110051.1:n.556-3211A>T
Search 100 bp 5'
Search 100 bp 3'