Canonical Allele Identifier: CA2589604659

Gene: CDC25B

Linked Data

• dbSNP Id: rs1600383692
• gnomAD v3: 20-3795544-A-G
• gnomAD v4: 20-3795544-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795544A>G , CM000682.2:g.3795544A>G	GRCh38
NC_000020.10:g.3776191A>G , CM000682.1:g.3776191A>G	GRCh37
NC_000020.9:g.3724191A>G	NCBI36
NG_029040.2:g.13773A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344256.10:c.9-2078A>G	ENSP00000339125.6:n.9-2078A>G
ENST00000379598.9:c.9-2078A>G	ENSP00000368918.5:n.9-2078A>G
NM_001287516.1:c.9-2078A>G	NP_001274445.1:n.9-2078A>G
NM_001287517.1:c.9-2120A>G	NP_001274446.1:n.9-2120A>G
NM_001287518.1:c.9-2078A>G	NP_001274447.1:n.9-2078A>G
NR_136336.1:n.369-2078A>G
NM_001287516.2:c.9-2078A>G	NP_001274445.1:n.9-2078A>G
NM_001287517.2:c.9-2120A>G	NP_001274446.1:n.9-2120A>G
NM_001287518.2:c.9-2078A>G	NP_001274447.1:n.9-2078A>G
NR_136336.2:n.190-2078A>G