Canonical Allele Identifier: CA15961708

Gene: ZNF217 ZNF217-AS1

Linked Data

• dbSNP Id: rs1056948
• gnomAD v2: 20-52183705-C-T
• gnomAD v3: 20-53567166-C-T
• gnomAD v4: 20-53567166-C-T
• MyVariant Identifiers: chr20:g.52183705C>T (hg19) ; chr20:g.53567166C>T (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.53567166C>T , CM000682.2:g.53567166C>T	GRCh38
NC_000020.10:g.52183705C>T , CM000682.1:g.52183705C>T	GRCh37
NC_000020.9:g.51617112C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371471.7:c.*2122G>A (ZNF217) MANE Select	ENSP00000360526.2:n.*2122G>A
ENST00000302342.3:c.*2122G>A (ZNF217)	ENSP00000304308.3:n.*2122G>A
ENST00000371471.6:c.*2122G>A (ZNF217)	ENSP00000360526.2:n.*2122G>A
NM_006526.2:c.*2122G>A (ZNF217)	NP_006517.1:n.*2122G>A
NR_110051.1:n.556-3106C>T (ZNF217-AS1)
XM_005260545.2:c.*1950G>A (ZNF217)	XP_005260602.1:n.*1950G>A
XM_006723875.2:c.*1950G>A (ZNF217)	XP_006723938.1:n.*1950G>A
XM_011529036.1:c.*1950G>A (ZNF217)	XP_011527338.1:n.*1950G>A
XM_005260545.4:c.*1950G>A (ZNF217)	XP_005260602.1:n.*1950G>A
XM_017028059.2:c.*2122G>A (ZNF217)	XP_016883548.1:n.*2122G>A
XM_024451996.1:c.*1950G>A (ZNF217)	XP_024307764.1:n.*1950G>A
XM_024451997.1:c.*1950G>A (ZNF217)	XP_024307765.1:n.*1950G>A
XM_024451998.1:c.*1950G>A (ZNF217)	XP_024307766.1:n.*1950G>A
NM_001385034.1:c.*1950G>A (ZNF217)	NP_001371963.1:n.*1950G>A
NM_006526.3:c.*2122G>A (ZNF217) MANE Select	NP_006517.1:n.*2122G>A