Canonical Allele Identifier: CA408592923

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395596G>A (hg19) ; chr20:g.32807790G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807790G>A , CM000682.2:g.32807790G>A	GRCh38
NC_000020.10:g.31395596G>A , CM000682.1:g.31395596G>A	GRCh37
NC_000020.9:g.30859257G>A	NCBI36
NG_007290.1:g.50406G>A , LRG_56:g.50406G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1400G>A	ENSP00000512497.1:n.*1400G>A
ENST00000696232.1:c.2260G>A	ENSP00000512498.1:p.Asp754Asn
ENST00000696233.1:c.*1003G>A	ENSP00000512499.1:n.*1003G>A
ENST00000696238.1:c.*1192G>A	ENSP00000512502.1:n.*1192G>A
ENST00000696239.1:c.2230G>A	ENSP00000512503.1:p.Asp744Asn
ENST00000696245.1:n.474G>A
ENST00000201963.3:c.2425G>A	ENSP00000201963.3:p.Asp809Asn
ENST00000328111.6:c.2449G>A MANE Select	ENSP00000328547.2:p.Asp817Asn
ENST00000348286.6:c.2200G>A	ENSP00000337764.2:p.Asp734Asn
ENST00000353855.6:c.2389G>A	ENSP00000313397.4:p.Asp797Asn
ENST00000443239.7:c.2074G>A	ENSP00000403169.2:p.Asp692Asn
ENST00000456297.6:c.1972G>A	ENSP00000412305.1:p.Asp658Asn
NM_001207055.1:c.2074G>A	NP_001193984.1:p.Asp692Asn
NM_001207056.1:c.1972G>A	NP_001193985.1:p.Asp658Asn
NM_006892.3:c.2449G>A , LRG_56t1:c.2449G>A	NP_008823.1:p.Asp817Asn
NM_175848.1:c.2389G>A	NP_787044.1:p.Asp797Asn
NM_175849.1:c.2200G>A	NP_787045.1:p.Asp734Asn
NM_175850.2:c.2425G>A	NP_787046.1:p.Asp809Asn
XM_011528653.1:c.2236G>A	XP_011526955.1:p.Asp746Asn
XM_011528654.1:c.2110G>A	XP_011526956.1:p.Asp704Asn
XR_936511.1:n.2227G>A
XM_011528653.2:c.2236G>A	XP_011526955.1:p.Asp746Asn
XM_011528654.2:c.2110G>A	XP_011526956.1:p.Asp704Asn
XR_936511.2:n.2238G>A
NM_001207055.2:c.2074G>A	NP_001193984.1:p.Asp692Asn
NM_001207056.2:c.1972G>A	NP_001193985.1:p.Asp658Asn
NM_006892.4:c.2449G>A MANE Select	NP_008823.1:p.Asp817Asn
NM_175848.2:c.2389G>A	NP_787044.1:p.Asp797Asn
NM_175849.2:c.2200G>A	NP_787045.1:p.Asp734Asn
NM_175850.3:c.2425G>A	NP_787046.1:p.Asp809Asn