Canonical Allele Identifier: CA2346738090
Gene: CDC25B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795543C= , CM000682.2:g.3795543C= GRCh38
NC_000020.10:g.3776190C= , CM000682.1:g.3776190C= GRCh37
NC_000020.9:g.3724190C= NCBI36
NG_029040.2:g.13772C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344256.10:c.9-2079C= ENSP00000339125.6:n.9-2079C=
ENST00000379598.9:c.9-2079C= ENSP00000368918.5:n.9-2079C=
NM_001287516.1:c.9-2079C= NP_001274445.1:n.9-2079C=
NM_001287517.1:c.9-2121C= NP_001274446.1:n.9-2121C=
NM_001287518.1:c.9-2079C= NP_001274447.1:n.9-2079C=
NR_136336.1:n.369-2079C=
NM_001287516.2:c.9-2079C= NP_001274445.1:n.9-2079C=
NM_001287517.2:c.9-2121C= NP_001274446.1:n.9-2121C=
NM_001287518.2:c.9-2079C= NP_001274447.1:n.9-2079C=
NR_136336.2:n.190-2079C=