Canonical Allele Identifier: CA408592808

Gene: DNMT3B

Linked Data

• COSMIC: COSM4962214 ; COSM4962215
• MyVariant Identifiers: chr20:g.31395568G>C (hg19) ; chr20:g.32807762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807762G>C , CM000682.2:g.32807762G>C	GRCh38
NC_000020.10:g.31395568G>C , CM000682.1:g.31395568G>C	GRCh37
NC_000020.9:g.30859229G>C	NCBI36
NG_007290.1:g.50378G>C , LRG_56:g.50378G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1372G>C	ENSP00000512497.1:n.*1372G>C
ENST00000696232.1:c.2232G>C	ENSP00000512498.1:p.Arg744Ser
ENST00000696233.1:c.*975G>C	ENSP00000512499.1:n.*975G>C
ENST00000696238.1:c.*1164G>C	ENSP00000512502.1:n.*1164G>C
ENST00000696239.1:c.2202G>C	ENSP00000512503.1:p.Arg734Ser
ENST00000696245.1:n.446G>C
ENST00000201963.3:c.2397G>C	ENSP00000201963.3:p.Arg799Ser
ENST00000328111.6:c.2421G>C MANE Select	ENSP00000328547.2:p.Arg807Ser
ENST00000348286.6:c.2172G>C	ENSP00000337764.2:p.Arg724Ser
ENST00000353855.6:c.2361G>C	ENSP00000313397.4:p.Arg787Ser
ENST00000443239.7:c.2046G>C	ENSP00000403169.2:p.Arg682Ser
ENST00000456297.6:c.1944G>C	ENSP00000412305.1:p.Arg648Ser
NM_001207055.1:c.2046G>C	NP_001193984.1:p.Arg682Ser
NM_001207056.1:c.1944G>C	NP_001193985.1:p.Arg648Ser
NM_006892.3:c.2421G>C , LRG_56t1:c.2421G>C	NP_008823.1:p.Arg807Ser
NM_175848.1:c.2361G>C	NP_787044.1:p.Arg787Ser
NM_175849.1:c.2172G>C	NP_787045.1:p.Arg724Ser
NM_175850.2:c.2397G>C	NP_787046.1:p.Arg799Ser
XM_011528653.1:c.2208G>C	XP_011526955.1:p.Arg736Ser
XM_011528654.1:c.2082G>C	XP_011526956.1:p.Arg694Ser
XR_936511.1:n.2199G>C
XM_011528653.2:c.2208G>C	XP_011526955.1:p.Arg736Ser
XM_011528654.2:c.2082G>C	XP_011526956.1:p.Arg694Ser
XR_936511.2:n.2210G>C
NM_001207055.2:c.2046G>C	NP_001193984.1:p.Arg682Ser
NM_001207056.2:c.1944G>C	NP_001193985.1:p.Arg648Ser
NM_006892.4:c.2421G>C MANE Select	NP_008823.1:p.Arg807Ser
NM_175848.2:c.2361G>C	NP_787044.1:p.Arg787Ser
NM_175849.2:c.2172G>C	NP_787045.1:p.Arg724Ser
NM_175850.3:c.2397G>C	NP_787046.1:p.Arg799Ser