Canonical Allele Identifier: CA745561431

Gene: ZNF217-AS1

Linked Data

• dbSNP Id: rs1202948725
• gnomAD v3: 20-53566900-T-C
• gnomAD v4: 20-53566900-T-C
• MyVariant Identifiers: chr20:g.52183439T>C (hg19) ; chr20:g.53566900T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.53566900T>C , CM000682.2:g.53566900T>C	GRCh38
NC_000020.10:g.52183439T>C , CM000682.1:g.52183439T>C	GRCh37
NC_000020.9:g.51616846T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110051.1:n.556-3372T>C