Canonical Allele Identifier: CA2346738039

Gene: CDC25B

Linked Data

• dbSNP Id: rs2089003951

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795441T>C , CM000682.2:g.3795441T>C	GRCh38
NC_000020.10:g.3776088T>C , CM000682.1:g.3776088T>C	GRCh37
NC_000020.9:g.3724088T>C	NCBI36
NG_029040.2:g.13670T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2181T>C	ENSP00000339125.6:n.9-2181T>C
ENST00000379598.9:c.9-2181T>C	ENSP00000368918.5:n.9-2181T>C
NM_001287516.1:c.9-2181T>C	NP_001274445.1:n.9-2181T>C
NM_001287517.1:c.9-2223T>C	NP_001274446.1:n.9-2223T>C
NM_001287518.1:c.9-2181T>C	NP_001274447.1:n.9-2181T>C
NR_136336.1:n.369-2181T>C
NM_001287516.2:c.9-2181T>C	NP_001274445.1:n.9-2181T>C
NM_001287517.2:c.9-2223T>C	NP_001274446.1:n.9-2223T>C
NM_001287518.2:c.9-2181T>C	NP_001274447.1:n.9-2181T>C
NR_136336.2:n.190-2181T>C