Canonical Allele Identifier: CA2346738091
Gene: CDC25B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3795544A= , CM000682.2:g.3795544A= GRCh38
NC_000020.10:g.3776191A= , CM000682.1:g.3776191A= GRCh37
NC_000020.9:g.3724191A= NCBI36
NG_029040.2:g.13773A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344256.10:c.9-2078A= ENSP00000339125.6:n.9-2078A=
ENST00000379598.9:c.9-2078A= ENSP00000368918.5:n.9-2078A=
NM_001287516.1:c.9-2078A= NP_001274445.1:n.9-2078A=
NM_001287517.1:c.9-2120A= NP_001274446.1:n.9-2120A=
NM_001287518.1:c.9-2078A= NP_001274447.1:n.9-2078A=
NR_136336.1:n.369-2078A=
NM_001287516.2:c.9-2078A= NP_001274445.1:n.9-2078A=
NM_001287517.2:c.9-2120A= NP_001274446.1:n.9-2120A=
NM_001287518.2:c.9-2078A= NP_001274447.1:n.9-2078A=
NR_136336.2:n.190-2078A=