Canonical Allele Identifier: CA2360456914
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787182_32787183delinsAC , CM000682.2:g.32787182_32787183delinsAC GRCh38
NC_000020.10:g.31374988_31374989delinsAC , CM000682.1:g.31374988_31374989delinsAC GRCh37
NC_000020.9:g.30838649_30838650delinsAC NCBI36
NG_007290.1:g.29798_29799delinsAC , LRG_56:g.29798_29799delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.433-48_433-47delinsAC ENSP00000512497.1:n.433-48_433-47delinsAC
ENST00000696232.1:c.433-48_433-47delinsAC ENSP00000512498.1:n.433-48_433-47delinsAC
ENST00000696233.1:c.433-48_433-47delinsAC ENSP00000512499.1:n.433-48_433-47delinsAC
ENST00000696234.1:n.417-48_417-47delinsAC
ENST00000696235.1:c.307-48_307-47delinsAC ENSP00000512500.1:n.307-48_307-47delinsAC
ENST00000696236.1:c.307-48_307-47delinsAC ENSP00000512501.1:n.307-48_307-47delinsAC
ENST00000696237.1:n.539-48_539-47delinsAC
ENST00000696238.1:c.433-48_433-47delinsAC ENSP00000512502.1:n.433-48_433-47delinsAC
ENST00000696239.1:c.433-48_433-47delinsAC ENSP00000512503.1:n.433-48_433-47delinsAC
ENST00000201963.3:c.469-48_469-47delinsAC ENSP00000201963.3:n.469-48_469-47delinsAC
ENST00000328111.6:c.433-48_433-47delinsAC MANE Select ENSP00000328547.2:n.433-48_433-47delinsAC
ENST00000348286.6:c.433-48_433-47delinsAC ENSP00000337764.2:n.433-48_433-47delinsAC
ENST00000353855.6:c.433-48_433-47delinsAC ENSP00000313397.4:n.433-48_433-47delinsAC
ENST00000443239.7:c.307-48_307-47delinsAC ENSP00000403169.2:n.307-48_307-47delinsAC
ENST00000456297.6:c.205-48_205-47delinsAC ENSP00000412305.1:n.205-48_205-47delinsAC
NM_001207055.1:c.307-48_307-47delinsAC NP_001193984.1:n.307-48_307-47delinsAC
NM_001207056.1:c.205-48_205-47delinsAC NP_001193985.1:n.205-48_205-47delinsAC
NM_006892.3:c.433-48_433-47delinsAC , LRG_56t1:c.433-48_433-47delinsAC NP_008823.1:n.433-48_433-47delinsAC
NM_175848.1:c.433-48_433-47delinsAC NP_787044.1:n.433-48_433-47delinsAC
NM_175849.1:c.433-48_433-47delinsAC NP_787045.1:n.433-48_433-47delinsAC
NM_175850.2:c.469-48_469-47delinsAC NP_787046.1:n.469-48_469-47delinsAC
XM_011528653.1:c.469-48_469-47delinsAC XP_011526955.1:n.469-48_469-47delinsAC
XM_011528654.1:c.343-48_343-47delinsAC XP_011526956.1:n.343-48_343-47delinsAC
XR_936510.1:n.605-48_605-47delinsAC
XR_936511.1:n.605-48_605-47delinsAC
XR_936512.1:n.480-48_480-47delinsAC
XM_011528653.2:c.469-48_469-47delinsAC XP_011526955.1:n.469-48_469-47delinsAC
XM_011528654.2:c.343-48_343-47delinsAC XP_011526956.1:n.343-48_343-47delinsAC
XR_936510.2:n.616-48_616-47delinsAC
XR_936511.2:n.616-48_616-47delinsAC
XR_936512.2:n.492-48_492-47delinsAC
NM_001207055.2:c.307-48_307-47delinsAC NP_001193984.1:n.307-48_307-47delinsAC
NM_001207056.2:c.205-48_205-47delinsAC NP_001193985.1:n.205-48_205-47delinsAC
NM_006892.4:c.433-48_433-47delinsAC MANE Select NP_008823.1:n.433-48_433-47delinsAC
NM_175848.2:c.433-48_433-47delinsAC NP_787044.1:n.433-48_433-47delinsAC
NM_175849.2:c.433-48_433-47delinsAC NP_787045.1:n.433-48_433-47delinsAC
NM_175850.3:c.469-48_469-47delinsAC NP_787046.1:n.469-48_469-47delinsAC