Canonical Allele Identifier: CA2346738103
Gene: CDC25B HGNC NCBI

Linked Data

dbSNP Id: rs2089007114
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795564G>A , CM000682.2:g.3795564G>A GRCh38
NC_000020.10:g.3776211G>A , CM000682.1:g.3776211G>A GRCh37
NC_000020.9:g.3724211G>A NCBI36
NG_029040.2:g.13793G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344256.10:c.9-2058G>A ENSP00000339125.6:n.9-2058G>A
ENST00000379598.9:c.9-2058G>A ENSP00000368918.5:n.9-2058G>A
NM_001287516.1:c.9-2058G>A NP_001274445.1:n.9-2058G>A
NM_001287517.1:c.9-2100G>A NP_001274446.1:n.9-2100G>A
NM_001287518.1:c.9-2058G>A NP_001274447.1:n.9-2058G>A
NR_136336.1:n.369-2058G>A
NM_001287516.2:c.9-2058G>A NP_001274445.1:n.9-2058G>A
NM_001287517.2:c.9-2100G>A NP_001274446.1:n.9-2100G>A
NM_001287518.2:c.9-2058G>A NP_001274447.1:n.9-2058G>A
NR_136336.2:n.190-2058G>A
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