Canonical Allele Identifier: CA2369989122
Gene: ZNF217 HGNC NCBI
ZNF217-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53567067A= , CM000682.2:g.53567067A= GRCh38
NC_000020.10:g.52183606A= , CM000682.1:g.52183606A= GRCh37
NC_000020.9:g.51617013A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371471.6:c.*2221T= (ZNF217) ENSP00000360526.2:n.*2221T=
NR_110051.1:n.556-3205A= (ZNF217-AS1)
XM_005260545.2:c.*2049T= (ZNF217) XP_005260602.1:n.*2049T=
XM_006723875.2:c.*2049T= (ZNF217) XP_006723938.1:n.*2049T=
XM_011529036.1:c.*2049T= (ZNF217) XP_011527338.1:n.*2049T=
XM_005260545.4:c.*2049T= (ZNF217) XP_005260602.1:n.*2049T=
XM_024451996.1:c.*2049T= (ZNF217) XP_024307764.1:n.*2049T=
XM_024451997.1:c.*2049T= (ZNF217) XP_024307765.1:n.*2049T=
XM_024451998.1:c.*2049T= (ZNF217) XP_024307766.1:n.*2049T=
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