Canonical Allele Identifier: CA163130685
Gene: ZSCAN25 HGNC NCBI

Linked Data

dbSNP Id: rs1028825645
MyVariant Identifiers: chr7:g.99642513C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99642513C>A , CM000669.2:g.99642513C>A GRCh38
NC_000007.13:g.99240136C>A , CM000669.1:g.99240136C>A GRCh37
NC_000007.12:g.99078072C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515909.1:c.805+18333C>A XP_011514211.1:n.805+18333C>A
XM_011515910.1:c.806-4958C>A XP_011514212.1:n.806-4958C>A
XR_927402.1:n.1466+18333C>A
NM_001350984.1:c.805+18333C>A NP_001337913.1:n.805+18333C>A
NM_001350985.1:c.805+18333C>A NP_001337914.1:n.805+18333C>A
XM_011515909.2:c.805+18333C>A XP_011514211.1:n.805+18333C>A
XM_011515910.2:c.806-4958C>A XP_011514212.1:n.806-4958C>A
XR_927402.2:n.1465+18333C>A
NM_001350984.2:c.805+18333C>A NP_001337913.1:n.805+18333C>A
NM_001350985.2:c.805+18333C>A NP_001337914.1:n.805+18333C>A