Canonical Allele Identifier: CA2346738044

Gene: CDC25B

Linked Data

• dbSNP Id: rs2089004190

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3795452_3795455del , CM000682.2:g.3795452_3795455del	GRCh38
NC_000020.10:g.3776099_3776102del , CM000682.1:g.3776099_3776102del	GRCh37
NC_000020.9:g.3724099_3724102del	NCBI36
NG_029040.2:g.13681_13684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344256.10:c.9-2170_9-2167del	ENSP00000339125.6:n.9-2170_9-2167del
ENST00000379598.9:c.9-2170_9-2167del	ENSP00000368918.5:n.9-2170_9-2167del
NM_001287516.1:c.9-2170_9-2167del	NP_001274445.1:n.9-2170_9-2167del
NM_001287517.1:c.9-2212_9-2209del	NP_001274446.1:n.9-2212_9-2209del
NM_001287518.1:c.9-2170_9-2167del	NP_001274447.1:n.9-2170_9-2167del
NR_136336.1:n.369-2170_369-2167del
NM_001287516.2:c.9-2170_9-2167del	NP_001274445.1:n.9-2170_9-2167del
NM_001287517.2:c.9-2212_9-2209del	NP_001274446.1:n.9-2212_9-2209del
NM_001287518.2:c.9-2170_9-2167del	NP_001274447.1:n.9-2170_9-2167del
NR_136336.2:n.190-2170_190-2167del