Canonical Allele Identifier: CA163130645

Gene: ZSCAN25

Linked Data

• dbSNP Id: rs1009679602
• MyVariant Identifiers: chr7:g.99642363C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99642363C>T , CM000669.2:g.99642363C>T	GRCh38
NC_000007.13:g.99239986C>T , CM000669.1:g.99239986C>T	GRCh37
NC_000007.12:g.99077922C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515909.1:c.805+18183C>T	XP_011514211.1:n.805+18183C>T
XM_011515910.1:c.806-5108C>T	XP_011514212.1:n.806-5108C>T
XR_927402.1:n.1466+18183C>T
NM_001350984.1:c.805+18183C>T	NP_001337913.1:n.805+18183C>T
NM_001350985.1:c.805+18183C>T	NP_001337914.1:n.805+18183C>T
XM_011515909.2:c.805+18183C>T	XP_011514211.1:n.805+18183C>T
XM_011515910.2:c.806-5108C>T	XP_011514212.1:n.806-5108C>T
XR_927402.2:n.1465+18183C>T
NM_001350984.2:c.805+18183C>T	NP_001337913.1:n.805+18183C>T
NM_001350985.2:c.805+18183C>T	NP_001337914.1:n.805+18183C>T