Canonical Allele Identifier: CA408592951

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395602T>C (hg19) ; chr20:g.32807796T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807796T>C , CM000682.2:g.32807796T>C	GRCh38
NC_000020.10:g.31395602T>C , CM000682.1:g.31395602T>C	GRCh37
NC_000020.9:g.30859263T>C	NCBI36
NG_007290.1:g.50412T>C , LRG_56:g.50412T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1406T>C	ENSP00000512497.1:n.*1406T>C
ENST00000696232.1:c.2266T>C	ENSP00000512498.1:p.Ser756Pro
ENST00000696233.1:c.*1009T>C	ENSP00000512499.1:n.*1009T>C
ENST00000696238.1:c.*1198T>C	ENSP00000512502.1:n.*1198T>C
ENST00000696239.1:c.2236T>C	ENSP00000512503.1:p.Ser746Pro
ENST00000696245.1:n.480T>C
ENST00000201963.3:c.2431T>C	ENSP00000201963.3:p.Ser811Pro
ENST00000328111.6:c.2455T>C MANE Select	ENSP00000328547.2:p.Ser819Pro
ENST00000348286.6:c.2206T>C	ENSP00000337764.2:p.Ser736Pro
ENST00000353855.6:c.2395T>C	ENSP00000313397.4:p.Ser799Pro
ENST00000443239.7:c.2080T>C	ENSP00000403169.2:p.Ser694Pro
ENST00000456297.6:c.1978T>C	ENSP00000412305.1:p.Ser660Pro
NM_001207055.1:c.2080T>C	NP_001193984.1:p.Ser694Pro
NM_001207056.1:c.1978T>C	NP_001193985.1:p.Ser660Pro
NM_006892.3:c.2455T>C , LRG_56t1:c.2455T>C	NP_008823.1:p.Ser819Pro
NM_175848.1:c.2395T>C	NP_787044.1:p.Ser799Pro
NM_175849.1:c.2206T>C	NP_787045.1:p.Ser736Pro
NM_175850.2:c.2431T>C	NP_787046.1:p.Ser811Pro
XM_011528653.1:c.2242T>C	XP_011526955.1:p.Ser748Pro
XM_011528654.1:c.2116T>C	XP_011526956.1:p.Ser706Pro
XR_936511.1:n.2233T>C
XM_011528653.2:c.2242T>C	XP_011526955.1:p.Ser748Pro
XM_011528654.2:c.2116T>C	XP_011526956.1:p.Ser706Pro
XR_936511.2:n.2244T>C
NM_001207055.2:c.2080T>C	NP_001193984.1:p.Ser694Pro
NM_001207056.2:c.1978T>C	NP_001193985.1:p.Ser660Pro
NM_006892.4:c.2455T>C MANE Select	NP_008823.1:p.Ser819Pro
NM_175848.2:c.2395T>C	NP_787044.1:p.Ser799Pro
NM_175849.2:c.2206T>C	NP_787045.1:p.Ser736Pro
NM_175850.3:c.2431T>C	NP_787046.1:p.Ser811Pro