Canonical Allele Identifier: CA576410118

Gene: ZSCAN25

Linked Data

• dbSNP Id: rs1332061692
• gnomAD v2: 7-99240029-A-T
• gnomAD v3: 7-99642406-A-T
• gnomAD v4: 7-99642406-A-T
• MyVariant Identifiers: chr7:g.99240029A>T (hg19) ; chr7:g.99642406A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99642406A>T , CM000669.2:g.99642406A>T	GRCh38
NC_000007.13:g.99240029A>T , CM000669.1:g.99240029A>T	GRCh37
NC_000007.12:g.99077965A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515909.1:c.805+18226A>T	XP_011514211.1:n.805+18226A>T
XM_011515910.1:c.806-5065A>T	XP_011514212.1:n.806-5065A>T
XR_927402.1:n.1466+18226A>T
NM_001350984.1:c.805+18226A>T	NP_001337913.1:n.805+18226A>T
NM_001350985.1:c.805+18226A>T	NP_001337914.1:n.805+18226A>T
XM_011515909.2:c.805+18226A>T	XP_011514211.1:n.805+18226A>T
XM_011515910.2:c.806-5065A>T	XP_011514212.1:n.806-5065A>T
XR_927402.2:n.1465+18226A>T
NM_001350984.2:c.805+18226A>T	NP_001337913.1:n.805+18226A>T
NM_001350985.2:c.805+18226A>T	NP_001337914.1:n.805+18226A>T