Canonical Allele Identifier: CA163130684
Gene: ZSCAN25 HGNC NCBI

Linked Data

dbSNP Id: rs997764847

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99642511C>T , CM000669.2:g.99642511C>T GRCh38
NC_000007.13:g.99240134C>T , CM000669.1:g.99240134C>T GRCh37
NC_000007.12:g.99078070C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515909.1:c.805+18331C>T XP_011514211.1:n.805+18331C>T
XM_011515910.1:c.806-4960C>T XP_011514212.1:n.806-4960C>T
XR_927402.1:n.1466+18331C>T
NM_001350984.1:c.805+18331C>T NP_001337913.1:n.805+18331C>T
NM_001350985.1:c.805+18331C>T NP_001337914.1:n.805+18331C>T
XM_011515909.2:c.805+18331C>T XP_011514211.1:n.805+18331C>T
XM_011515910.2:c.806-4960C>T XP_011514212.1:n.806-4960C>T
XR_927402.2:n.1465+18331C>T
NM_001350984.2:c.805+18331C>T NP_001337913.1:n.805+18331C>T
NM_001350985.2:c.805+18331C>T NP_001337914.1:n.805+18331C>T