Canonical Allele Identifier: CA993601790

Gene: ZNF788P ZNF20

Linked Data

• dbSNP Id: rs1976457728
• gnomAD v3: 19-12114664-G-C
• gnomAD v4: 19-12114664-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12114664G>C , CM000681.2:g.12114664G>C	GRCh38
NC_000019.9:g.12225479G>C , CM000681.1:g.12225479G>C	GRCh37
NC_000019.8:g.12086479G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430298.6:c.*3360G>C (ZNF788P)	ENSP00000391703.1:n.*3360G>C
ENST00000600335.5:c.191+20836C>G (ZNF20)	ENSP00000470025.1:n.191+20836C>G
ENST00000601686.1:n.165-21111G>C (ZNF788P)
NR_027049.1:n.3754G>C (ZNF788P)
NM_001348163.1:c.*1269G>C (ZNF788P)	NP_001335092.1:n.*1269G>C
NM_001348164.1:c.*1269G>C (ZNF788P)	NP_001335093.1:n.*1269G>C
NM_001348165.1:c.*1269G>C (ZNF788P)	NP_001335094.1:n.*1269G>C
XM_024451502.1:c.*1269G>C (ZNF788P)	XP_024307270.1:n.*1269G>C
NM_001348163.2:c.*1269G>C (ZNF788P)	NP_001335092.1:n.*1269G>C
NM_001348164.2:c.*1269G>C (ZNF788P)	NP_001335093.1:n.*1269G>C
NM_001348165.2:c.*1269G>C (ZNF788P)	NP_001335094.1:n.*1269G>C
NR_171037.1:n.3780G>C (ZNF788P)
NR_171038.1:n.3593G>C (ZNF788P)
NR_171039.1:n.3720G>C (ZNF788P)
NR_171040.1:n.3841G>C (ZNF788P)
NR_171041.1:n.3714G>C (ZNF788P)
NR_171042.1:n.3654G>C (ZNF788P)
NR_171043.1:n.3781G>C (ZNF788P)