Canonical Allele Identifier: CA316149249
Gene: ZNF217-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs958485463
MyVariant Identifiers: chr20:g.52183449C>A (hg19) chr20:g.53566910C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53566910C>A , CM000682.2:g.53566910C>A GRCh38
NC_000020.10:g.52183449C>A , CM000682.1:g.52183449C>A GRCh37
NC_000020.9:g.51616856C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110051.1:n.556-3362C>A
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