Canonical Allele Identifier: CA311014713

Gene: CDC25B

Linked Data

• dbSNP Id: rs1023311933
• MyVariant Identifiers: chr20:g.3776084G>T (hg19) ; chr20:g.3795437G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795437G>T , CM000682.2:g.3795437G>T	GRCh38
NC_000020.10:g.3776084G>T , CM000682.1:g.3776084G>T	GRCh37
NC_000020.9:g.3724084G>T	NCBI36
NG_029040.2:g.13666G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2185G>T	ENSP00000339125.6:n.9-2185G>T
ENST00000379598.9:c.9-2185G>T	ENSP00000368918.5:n.9-2185G>T
NM_001287516.1:c.9-2185G>T	NP_001274445.1:n.9-2185G>T
NM_001287517.1:c.9-2227G>T	NP_001274446.1:n.9-2227G>T
NM_001287518.1:c.9-2185G>T	NP_001274447.1:n.9-2185G>T
NR_136336.1:n.369-2185G>T
NM_001287516.2:c.9-2185G>T	NP_001274445.1:n.9-2185G>T
NM_001287517.2:c.9-2227G>T	NP_001274446.1:n.9-2227G>T
NM_001287518.2:c.9-2185G>T	NP_001274447.1:n.9-2185G>T
NR_136336.2:n.190-2185G>T