Canonical Allele Identifier: CA311014715

Gene: CDC25B

Linked Data

• dbSNP Id: rs990688072
• gnomAD v2: 20-3776112-A-G
• gnomAD v3: 20-3795465-A-G
• gnomAD v4: 20-3795465-A-G
• MyVariant Identifiers: chr20:g.3776112A>G (hg19) ; chr20:g.3795465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795465A>G , CM000682.2:g.3795465A>G	GRCh38
NC_000020.10:g.3776112A>G , CM000682.1:g.3776112A>G	GRCh37
NC_000020.9:g.3724112A>G	NCBI36
NG_029040.2:g.13694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2157A>G	ENSP00000339125.6:n.9-2157A>G
ENST00000379598.9:c.9-2157A>G	ENSP00000368918.5:n.9-2157A>G
NM_001287516.1:c.9-2157A>G	NP_001274445.1:n.9-2157A>G
NM_001287517.1:c.9-2199A>G	NP_001274446.1:n.9-2199A>G
NM_001287518.1:c.9-2157A>G	NP_001274447.1:n.9-2157A>G
NR_136336.1:n.369-2157A>G
NM_001287516.2:c.9-2157A>G	NP_001274445.1:n.9-2157A>G
NM_001287517.2:c.9-2199A>G	NP_001274446.1:n.9-2199A>G
NM_001287518.2:c.9-2157A>G	NP_001274447.1:n.9-2157A>G
NR_136336.2:n.190-2157A>G