Canonical Allele Identifier: CA408593029

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395620G>C (hg19) ; chr20:g.32807814G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807814G>C , CM000682.2:g.32807814G>C	GRCh38
NC_000020.10:g.31395620G>C , CM000682.1:g.31395620G>C	GRCh37
NC_000020.9:g.30859281G>C	NCBI36
NG_007290.1:g.50430G>C , LRG_56:g.50430G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1424G>C	ENSP00000512497.1:n.*1424G>C
ENST00000696232.1:c.2284G>C	ENSP00000512498.1:p.Ala762Pro
ENST00000696233.1:c.*1027G>C	ENSP00000512499.1:n.*1027G>C
ENST00000696238.1:c.*1216G>C	ENSP00000512502.1:n.*1216G>C
ENST00000696239.1:c.2254G>C	ENSP00000512503.1:p.Ala752Pro
ENST00000696245.1:n.498G>C
ENST00000201963.3:c.2449G>C	ENSP00000201963.3:p.Ala817Pro
ENST00000328111.6:c.2473G>C MANE Select	ENSP00000328547.2:p.Ala825Pro
ENST00000348286.6:c.2224G>C	ENSP00000337764.2:p.Ala742Pro
ENST00000353855.6:c.2413G>C	ENSP00000313397.4:p.Ala805Pro
ENST00000443239.7:c.2098G>C	ENSP00000403169.2:p.Ala700Pro
ENST00000456297.6:c.1996G>C	ENSP00000412305.1:p.Ala666Pro
NM_001207055.1:c.2098G>C	NP_001193984.1:p.Ala700Pro
NM_001207056.1:c.1996G>C	NP_001193985.1:p.Ala666Pro
NM_006892.3:c.2473G>C , LRG_56t1:c.2473G>C	NP_008823.1:p.Ala825Pro
NM_175848.1:c.2413G>C	NP_787044.1:p.Ala805Pro
NM_175849.1:c.2224G>C	NP_787045.1:p.Ala742Pro
NM_175850.2:c.2449G>C	NP_787046.1:p.Ala817Pro
XM_011528653.1:c.2260G>C	XP_011526955.1:p.Ala754Pro
XM_011528654.1:c.2134G>C	XP_011526956.1:p.Ala712Pro
XR_936511.1:n.2251G>C
XM_011528653.2:c.2260G>C	XP_011526955.1:p.Ala754Pro
XM_011528654.2:c.2134G>C	XP_011526956.1:p.Ala712Pro
XR_936511.2:n.2262G>C
NM_001207055.2:c.2098G>C	NP_001193984.1:p.Ala700Pro
NM_001207056.2:c.1996G>C	NP_001193985.1:p.Ala666Pro
NM_006892.4:c.2473G>C MANE Select	NP_008823.1:p.Ala825Pro
NM_175848.2:c.2413G>C	NP_787044.1:p.Ala805Pro
NM_175849.2:c.2224G>C	NP_787045.1:p.Ala742Pro
NM_175850.3:c.2449G>C	NP_787046.1:p.Ala817Pro