Canonical Allele Identifier: CA316149390
Gene: ZNF217 HGNC NCBI
ZNF217-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs547362391
gnomAD v3: 20-53567068-A-C
gnomAD v4: 20-53567068-A-C
MyVariant Identifiers: chr20:g.52183607A>C (hg19) chr20:g.53567068A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53567068A>C , CM000682.2:g.53567068A>C GRCh38
NC_000020.10:g.52183607A>C , CM000682.1:g.52183607A>C GRCh37
NC_000020.9:g.51617014A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371471.6:c.*2220T>G (ZNF217) ENSP00000360526.2:n.*2220T>G
NR_110051.1:n.556-3204A>C (ZNF217-AS1)
XM_005260545.2:c.*2048T>G (ZNF217) XP_005260602.1:n.*2048T>G
XM_006723875.2:c.*2048T>G (ZNF217) XP_006723938.1:n.*2048T>G
XM_011529036.1:c.*2048T>G (ZNF217) XP_011527338.1:n.*2048T>G
XM_005260545.4:c.*2048T>G (ZNF217) XP_005260602.1:n.*2048T>G
XM_024451996.1:c.*2048T>G (ZNF217) XP_024307764.1:n.*2048T>G
XM_024451997.1:c.*2048T>G (ZNF217) XP_024307765.1:n.*2048T>G
XM_024451998.1:c.*2048T>G (ZNF217) XP_024307766.1:n.*2048T>G
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