Canonical Allele Identifier: CA311014728

Gene: CDC25B

Linked Data

• dbSNP Id: rs1028478806
• gnomAD v3: 20-3795559-C-T
• gnomAD v4: 20-3795559-C-T
• MyVariant Identifiers: chr20:g.3776206C>T (hg19) ; chr20:g.3795559C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795559C>T , CM000682.2:g.3795559C>T	GRCh38
NC_000020.10:g.3776206C>T , CM000682.1:g.3776206C>T	GRCh37
NC_000020.9:g.3724206C>T	NCBI36
NG_029040.2:g.13788C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344256.10:c.9-2063C>T	ENSP00000339125.6:n.9-2063C>T
ENST00000379598.9:c.9-2063C>T	ENSP00000368918.5:n.9-2063C>T
NM_001287516.1:c.9-2063C>T	NP_001274445.1:n.9-2063C>T
NM_001287517.1:c.9-2105C>T	NP_001274446.1:n.9-2105C>T
NM_001287518.1:c.9-2063C>T	NP_001274447.1:n.9-2063C>T
NR_136336.1:n.369-2063C>T
NM_001287516.2:c.9-2063C>T	NP_001274445.1:n.9-2063C>T
NM_001287517.2:c.9-2105C>T	NP_001274446.1:n.9-2105C>T
NM_001287518.2:c.9-2063C>T	NP_001274447.1:n.9-2063C>T
NR_136336.2:n.190-2063C>T