Canonical Allele Identifier: CA408593062

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395636T>C (hg19) ; chr20:g.32807830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807830T>C , CM000682.2:g.32807830T>C	GRCh38
NC_000020.10:g.31395636T>C , CM000682.1:g.31395636T>C	GRCh37
NC_000020.9:g.30859297T>C	NCBI36
NG_007290.1:g.50446T>C , LRG_56:g.50446T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1440T>C	ENSP00000512497.1:n.*1440T>C
ENST00000696232.1:c.2300T>C	ENSP00000512498.1:p.Leu767Pro
ENST00000696233.1:c.*1043T>C	ENSP00000512499.1:n.*1043T>C
ENST00000696238.1:c.*1232T>C	ENSP00000512502.1:n.*1232T>C
ENST00000696239.1:c.2270T>C	ENSP00000512503.1:p.Leu757Pro
ENST00000696245.1:n.514T>C
ENST00000201963.3:c.2465T>C	ENSP00000201963.3:p.Leu822Pro
ENST00000328111.6:c.2489T>C MANE Select	ENSP00000328547.2:p.Leu830Pro
ENST00000348286.6:c.2240T>C	ENSP00000337764.2:p.Leu747Pro
ENST00000353855.6:c.2429T>C	ENSP00000313397.4:p.Leu810Pro
ENST00000443239.7:c.2114T>C	ENSP00000403169.2:p.Leu705Pro
ENST00000456297.6:c.2012T>C	ENSP00000412305.1:p.Leu671Pro
NM_001207055.1:c.2114T>C	NP_001193984.1:p.Leu705Pro
NM_001207056.1:c.2012T>C	NP_001193985.1:p.Leu671Pro
NM_006892.3:c.2489T>C , LRG_56t1:c.2489T>C	NP_008823.1:p.Leu830Pro
NM_175848.1:c.2429T>C	NP_787044.1:p.Leu810Pro
NM_175849.1:c.2240T>C	NP_787045.1:p.Leu747Pro
NM_175850.2:c.2465T>C	NP_787046.1:p.Leu822Pro
XM_011528653.1:c.2276T>C	XP_011526955.1:p.Leu759Pro
XM_011528654.1:c.2150T>C	XP_011526956.1:p.Leu717Pro
XR_936511.1:n.2267T>C
XM_011528653.2:c.2276T>C	XP_011526955.1:p.Leu759Pro
XM_011528654.2:c.2150T>C	XP_011526956.1:p.Leu717Pro
XR_936511.2:n.2278T>C
NM_001207055.2:c.2114T>C	NP_001193984.1:p.Leu705Pro
NM_001207056.2:c.2012T>C	NP_001193985.1:p.Leu671Pro
NM_006892.4:c.2489T>C MANE Select	NP_008823.1:p.Leu830Pro
NM_175848.2:c.2429T>C	NP_787044.1:p.Leu810Pro
NM_175849.2:c.2240T>C	NP_787045.1:p.Leu747Pro
NM_175850.3:c.2465T>C	NP_787046.1:p.Leu822Pro