Canonical Allele Identifier: CA2346738048

Gene: CDC25B

Linked Data

• dbSNP Id: rs2089004424

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795461A>G , CM000682.2:g.3795461A>G	GRCh38
NC_000020.10:g.3776108A>G , CM000682.1:g.3776108A>G	GRCh37
NC_000020.9:g.3724108A>G	NCBI36
NG_029040.2:g.13690A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344256.10:c.9-2161A>G	ENSP00000339125.6:n.9-2161A>G
ENST00000379598.9:c.9-2161A>G	ENSP00000368918.5:n.9-2161A>G
NM_001287516.1:c.9-2161A>G	NP_001274445.1:n.9-2161A>G
NM_001287517.1:c.9-2203A>G	NP_001274446.1:n.9-2203A>G
NM_001287518.1:c.9-2161A>G	NP_001274447.1:n.9-2161A>G
NR_136336.1:n.369-2161A>G
NM_001287516.2:c.9-2161A>G	NP_001274445.1:n.9-2161A>G
NM_001287517.2:c.9-2203A>G	NP_001274446.1:n.9-2203A>G
NM_001287518.2:c.9-2161A>G	NP_001274447.1:n.9-2161A>G
NR_136336.2:n.190-2161A>G