Canonical Allele Identifier: CA2346738105
Gene: CDC25B HGNC NCBI

Linked Data

dbSNP Id: rs2089007198

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795567del , CM000682.2:g.3795567del GRCh38
NC_000020.10:g.3776214del , CM000682.1:g.3776214del GRCh37
NC_000020.9:g.3724214del NCBI36
NG_029040.2:g.13796del

Transcript Alleles

HGVS Amino-acid change
ENST00000344256.10:c.9-2055del ENSP00000339125.6:n.9-2055del
ENST00000379598.9:c.9-2055del ENSP00000368918.5:n.9-2055del
NM_001287516.1:c.9-2055del NP_001274445.1:n.9-2055del
NM_001287517.1:c.9-2097del NP_001274446.1:n.9-2097del
NM_001287518.1:c.9-2055del NP_001274447.1:n.9-2055del
NR_136336.1:n.369-2055del
NM_001287516.2:c.9-2055del NP_001274445.1:n.9-2055del
NM_001287517.2:c.9-2097del NP_001274446.1:n.9-2097del
NM_001287518.2:c.9-2055del NP_001274447.1:n.9-2055del
NR_136336.2:n.190-2055del