Canonical Allele Identifier: CA634191620

Gene: CDC25B

Linked Data

• dbSNP Id: rs1390096000
• gnomAD v2: 20-3776083-T-A
• gnomAD v3: 20-3795436-T-A
• gnomAD v4: 20-3795436-T-A
• MyVariant Identifiers: chr20:g.3776083T>A (hg19) ; chr20:g.3795436T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795436T>A , CM000682.2:g.3795436T>A	GRCh38
NC_000020.10:g.3776083T>A , CM000682.1:g.3776083T>A	GRCh37
NC_000020.9:g.3724083T>A	NCBI36
NG_029040.2:g.13665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2186T>A	ENSP00000339125.6:n.9-2186T>A
ENST00000379598.9:c.9-2186T>A	ENSP00000368918.5:n.9-2186T>A
NM_001287516.1:c.9-2186T>A	NP_001274445.1:n.9-2186T>A
NM_001287517.1:c.9-2228T>A	NP_001274446.1:n.9-2228T>A
NM_001287518.1:c.9-2186T>A	NP_001274447.1:n.9-2186T>A
NR_136336.1:n.369-2186T>A
NM_001287516.2:c.9-2186T>A	NP_001274445.1:n.9-2186T>A
NM_001287517.2:c.9-2228T>A	NP_001274446.1:n.9-2228T>A
NM_001287518.2:c.9-2186T>A	NP_001274447.1:n.9-2186T>A
NR_136336.2:n.190-2186T>A