Canonical Allele Identifier: CA2346738089

Gene: CDC25B

Linked Data

• dbSNP Id: rs2089006493

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795540T>A , CM000682.2:g.3795540T>A	GRCh38
NC_000020.10:g.3776187T>A , CM000682.1:g.3776187T>A	GRCh37
NC_000020.9:g.3724187T>A	NCBI36
NG_029040.2:g.13769T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2082T>A	ENSP00000339125.6:n.9-2082T>A
ENST00000379598.9:c.9-2082T>A	ENSP00000368918.5:n.9-2082T>A
NM_001287516.1:c.9-2082T>A	NP_001274445.1:n.9-2082T>A
NM_001287517.1:c.9-2124T>A	NP_001274446.1:n.9-2124T>A
NM_001287518.1:c.9-2082T>A	NP_001274447.1:n.9-2082T>A
NR_136336.1:n.369-2082T>A
NM_001287516.2:c.9-2082T>A	NP_001274445.1:n.9-2082T>A
NM_001287517.2:c.9-2124T>A	NP_001274446.1:n.9-2124T>A
NM_001287518.2:c.9-2082T>A	NP_001274447.1:n.9-2082T>A
NR_136336.2:n.190-2082T>A