Canonical Allele Identifier: CA2323251782

Gene: ZNF788P ZNF20

Linked Data

• dbSNP Id: rs1976456301
• gnomAD v4: 19-12114626-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114626A>G , CM000681.2:g.12114626A>G	GRCh38
NC_000019.9:g.12225441A>G , CM000681.1:g.12225441A>G	GRCh37
NC_000019.8:g.12086441A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3322A>G (ZNF788P)	ENSP00000391703.1:n.*3322A>G
ENST00000600335.5:c.191+20874T>C (ZNF20)	ENSP00000470025.1:n.191+20874T>C
ENST00000601686.1:n.165-21149A>G (ZNF788P)
NR_027049.1:n.3716A>G (ZNF788P)
NM_001348163.1:c.*1231A>G (ZNF788P)	NP_001335092.1:n.*1231A>G
NM_001348164.1:c.*1231A>G (ZNF788P)	NP_001335093.1:n.*1231A>G
NM_001348165.1:c.*1231A>G (ZNF788P)	NP_001335094.1:n.*1231A>G
XM_024451502.1:c.*1231A>G (ZNF788P)	XP_024307270.1:n.*1231A>G
NM_001348163.2:c.*1231A>G (ZNF788P)	NP_001335092.1:n.*1231A>G
NM_001348164.2:c.*1231A>G (ZNF788P)	NP_001335093.1:n.*1231A>G
NM_001348165.2:c.*1231A>G (ZNF788P)	NP_001335094.1:n.*1231A>G
NR_171037.1:n.3742A>G (ZNF788P)
NR_171038.1:n.3555A>G (ZNF788P)
NR_171039.1:n.3682A>G (ZNF788P)
NR_171040.1:n.3803A>G (ZNF788P)
NR_171041.1:n.3676A>G (ZNF788P)
NR_171042.1:n.3616A>G (ZNF788P)
NR_171043.1:n.3743A>G (ZNF788P)