Canonical Allele Identifier: CA2346738093
Gene: CDC25B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795545C= , CM000682.2:g.3795545C= GRCh38
NC_000020.10:g.3776192C= , CM000682.1:g.3776192C= GRCh37
NC_000020.9:g.3724192C= NCBI36
NG_029040.2:g.13774C=

Transcript Alleles

HGVS Amino-acid change
ENST00000344256.10:c.9-2077C= ENSP00000339125.6:n.9-2077C=
ENST00000379598.9:c.9-2077C= ENSP00000368918.5:n.9-2077C=
NM_001287516.1:c.9-2077C= NP_001274445.1:n.9-2077C=
NM_001287517.1:c.9-2119C= NP_001274446.1:n.9-2119C=
NM_001287518.1:c.9-2077C= NP_001274447.1:n.9-2077C=
NR_136336.1:n.369-2077C=
NM_001287516.2:c.9-2077C= NP_001274445.1:n.9-2077C=
NM_001287517.2:c.9-2119C= NP_001274446.1:n.9-2119C=
NM_001287518.2:c.9-2077C= NP_001274447.1:n.9-2077C=
NR_136336.2:n.190-2077C=