Canonical Allele Identifier: CA1014891810

Gene: CDC25B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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