Canonical Allele Identifier: CA2736134363

Gene: CDC25B

Linked Data

• dbSNP Id: rs1053744639

Genomic Alleles

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

Transcript Alleles

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