Canonical Allele Identifier: CA185464325

Gene: ZNF572

Linked Data

• dbSNP Id: rs566775591
• gnomAD v3: 8-124929269-T-C
• gnomAD v4: 8-124929269-T-C
• MyVariant Identifiers: chr8:g.125941511T>C (hg19) ; chr8:g.124929269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.124929269T>C , CM000670.2:g.124929269T>C	GRCh38
NC_000008.10:g.125941511T>C , CM000670.1:g.125941511T>C	GRCh37
NC_000008.9:g.126010692T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011516828.1:c.4-12194T>C	XP_011515130.1:n.4-12194T>C
XR_928288.1:n.1074-12194T>C
XR_928289.1:n.1080-12194T>C
XR_928290.1:n.1072-12194T>C
XR_928291.1:n.1073-12194T>C
XR_928292.1:n.1083-12194T>C
XR_928293.1:n.1073-12194T>C
XR_928294.1:n.1116-12194T>C
XR_928295.1:n.1071-12194T>C
XR_928296.1:n.328-12194T>C
XR_928297.1:n.1116-12194T>C