Canonical Allele Identifier: CA2736126237
Gene: CDC25B HGNC NCBI

Linked Data

dbSNP Id: rs927912094

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795434C>T , CM000682.2:g.3795434C>T GRCh38
NC_000020.10:g.3776081C>T , CM000682.1:g.3776081C>T GRCh37
NC_000020.9:g.3724081C>T NCBI36
NG_029040.2:g.13663C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344256.10:c.9-2188C>T ENSP00000339125.6:n.9-2188C>T
ENST00000379598.9:c.9-2188C>T ENSP00000368918.5:n.9-2188C>T
NM_001287516.1:c.9-2188C>T NP_001274445.1:n.9-2188C>T
NM_001287517.1:c.9-2230C>T NP_001274446.1:n.9-2230C>T
NM_001287518.1:c.9-2188C>T NP_001274447.1:n.9-2188C>T
NR_136336.1:n.369-2188C>T
NM_001287516.2:c.9-2188C>T NP_001274445.1:n.9-2188C>T
NM_001287517.2:c.9-2230C>T NP_001274446.1:n.9-2230C>T
NM_001287518.2:c.9-2188C>T NP_001274447.1:n.9-2188C>T
NR_136336.2:n.190-2188C>T