Canonical Allele Identifier: CA1104970129
Gene: ZSCAN25 HGNC NCBI

Linked Data

dbSNP Id: rs1562978988
gnomAD v3: 7-99642475-G-T
gnomAD v4: 7-99642475-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99642475G>T , CM000669.2:g.99642475G>T GRCh38
NC_000007.13:g.99240098G>T , CM000669.1:g.99240098G>T GRCh37
NC_000007.12:g.99078034G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515909.1:c.805+18295G>T XP_011514211.1:n.805+18295G>T
XM_011515910.1:c.806-4996G>T XP_011514212.1:n.806-4996G>T
XR_927402.1:n.1466+18295G>T
NM_001350984.1:c.805+18295G>T NP_001337913.1:n.805+18295G>T
NM_001350985.1:c.805+18295G>T NP_001337914.1:n.805+18295G>T
XM_011515909.2:c.805+18295G>T XP_011514211.1:n.805+18295G>T
XM_011515910.2:c.806-4996G>T XP_011514212.1:n.806-4996G>T
XR_927402.2:n.1465+18295G>T
NM_001350984.2:c.805+18295G>T NP_001337913.1:n.805+18295G>T
NM_001350985.2:c.805+18295G>T NP_001337914.1:n.805+18295G>T