Canonical Allele Identifier: CA2369989195
Gene: ZNF217 HGNC NCBI
ZNF217-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1987779114

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.53567192A>T , CM000682.2:g.53567192A>T GRCh38
NC_000020.10:g.52183731A>T , CM000682.1:g.52183731A>T GRCh37
NC_000020.9:g.51617138A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371471.7:c.*2096T>A (ZNF217) MANE Select ENSP00000360526.2:n.*2096T>A
ENST00000302342.3:c.*2096T>A (ZNF217) ENSP00000304308.3:n.*2096T>A
ENST00000371471.6:c.*2096T>A (ZNF217) ENSP00000360526.2:n.*2096T>A
NM_006526.2:c.*2096T>A (ZNF217) NP_006517.1:n.*2096T>A
NR_110051.1:n.556-3080A>T (ZNF217-AS1)
XM_005260545.2:c.*1924T>A (ZNF217) XP_005260602.1:n.*1924T>A
XM_006723875.2:c.*1924T>A (ZNF217) XP_006723938.1:n.*1924T>A
XM_011529036.1:c.*1924T>A (ZNF217) XP_011527338.1:n.*1924T>A
XM_005260545.4:c.*1924T>A (ZNF217) XP_005260602.1:n.*1924T>A
XM_017028059.2:c.*2096T>A (ZNF217) XP_016883548.1:n.*2096T>A
XM_024451996.1:c.*1924T>A (ZNF217) XP_024307764.1:n.*1924T>A
XM_024451997.1:c.*1924T>A (ZNF217) XP_024307765.1:n.*1924T>A
XM_024451998.1:c.*1924T>A (ZNF217) XP_024307766.1:n.*1924T>A
NM_001385034.1:c.*1924T>A (ZNF217) NP_001371963.1:n.*1924T>A
NM_006526.3:c.*2096T>A (ZNF217) MANE Select NP_006517.1:n.*2096T>A