Allele Registry

Canonical Allele Identifier: CA12594311

Gene: ZSCAN25 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr7:g.99735325T>G

GRCh37 chr7:g.99332948T>G

Linked Data - Sequence & Population

gnomAD v2:

7:99332948 T / G

gnomAD v3:

7:99735325 T / G

gnomAD v4:

chr7-99735325-T-G

Joint Max Group AF 0.03405831 (NFE)

Genomes Max Group AF 0.03434776 (NFE)

Exomes Max Group AF 0.03372936 (NFE)

Linked Data - NCBI & NCI

dbSNP:

45446698

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99735325T>G , CM000669.2:g.99735325T>G	GRCh38
NC_000007.13:g.99332948T>G , CM000669.1:g.99332948T>G	GRCh37
NC_000007.12:g.99170884T>G	NCBI36
NG_007983.1:g.4874A>C

Transcript Alleles

HGVS	Amino-acid Change
XR_927402.1:n.1788-1367T>G
XR_927402.2:n.1787-1367T>G

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