Canonical Allele Identifier: CA2346738056
Gene: CDC25B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795480T= , CM000682.2:g.3795480T= GRCh38
NC_000020.10:g.3776127T= , CM000682.1:g.3776127T= GRCh37
NC_000020.9:g.3724127T= NCBI36
NG_029040.2:g.13709T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344256.10:c.9-2142T= ENSP00000339125.6:n.9-2142T=
ENST00000379598.9:c.9-2142T= ENSP00000368918.5:n.9-2142T=
NM_001287516.1:c.9-2142T= NP_001274445.1:n.9-2142T=
NM_001287517.1:c.9-2184T= NP_001274446.1:n.9-2184T=
NM_001287518.1:c.9-2142T= NP_001274447.1:n.9-2142T=
NR_136336.1:n.369-2142T=
NM_001287516.2:c.9-2142T= NP_001274445.1:n.9-2142T=
NM_001287517.2:c.9-2184T= NP_001274446.1:n.9-2184T=
NM_001287518.2:c.9-2142T= NP_001274447.1:n.9-2142T=
NR_136336.2:n.190-2142T=