Canonical Allele Identifier: CA744125581

Gene: CDC25B

Linked Data

• dbSNP Id: rs1471158019
• gnomAD v3: 20-3795485-A-C
• gnomAD v4: 20-3795485-A-C
• MyVariant Identifiers: chr20:g.3776132A>C (hg19) ; chr20:g.3795485A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795485A>C , CM000682.2:g.3795485A>C	GRCh38
NC_000020.10:g.3776132A>C , CM000682.1:g.3776132A>C	GRCh37
NC_000020.9:g.3724132A>C	NCBI36
NG_029040.2:g.13714A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344256.10:c.9-2137A>C	ENSP00000339125.6:n.9-2137A>C
ENST00000379598.9:c.9-2137A>C	ENSP00000368918.5:n.9-2137A>C
NM_001287516.1:c.9-2137A>C	NP_001274445.1:n.9-2137A>C
NM_001287517.1:c.9-2179A>C	NP_001274446.1:n.9-2179A>C
NM_001287518.1:c.9-2137A>C	NP_001274447.1:n.9-2137A>C
NR_136336.1:n.369-2137A>C
NM_001287516.2:c.9-2137A>C	NP_001274445.1:n.9-2137A>C
NM_001287517.2:c.9-2179A>C	NP_001274446.1:n.9-2179A>C
NM_001287518.2:c.9-2137A>C	NP_001274447.1:n.9-2137A>C
NR_136336.2:n.190-2137A>C