Canonical Allele Identifier: CA408593123

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32807850-C-G
• MyVariant Identifiers: chr20:g.31395656C>G (hg19) ; chr20:g.32807850C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807850C>G , CM000682.2:g.32807850C>G	GRCh38
NC_000020.10:g.31395656C>G , CM000682.1:g.31395656C>G	GRCh37
NC_000020.9:g.30859317C>G	NCBI36
NG_007290.1:g.50466C>G , LRG_56:g.50466C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1460C>G	ENSP00000512497.1:n.*1460C>G
ENST00000696232.1:c.2320C>G	ENSP00000512498.1:p.Pro774Ala
ENST00000696233.1:c.*1063C>G	ENSP00000512499.1:n.*1063C>G
ENST00000696238.1:c.*1252C>G	ENSP00000512502.1:n.*1252C>G
ENST00000696239.1:c.2290C>G	ENSP00000512503.1:p.Pro764Ala
ENST00000696245.1:n.534C>G
ENST00000201963.3:c.2485C>G	ENSP00000201963.3:p.Pro829Ala
ENST00000328111.6:c.2509C>G MANE Select	ENSP00000328547.2:p.Pro837Ala
ENST00000348286.6:c.2260C>G	ENSP00000337764.2:p.Pro754Ala
ENST00000353855.6:c.2449C>G	ENSP00000313397.4:p.Pro817Ala
ENST00000443239.7:c.2134C>G	ENSP00000403169.2:p.Pro712Ala
ENST00000456297.6:c.2032C>G	ENSP00000412305.1:p.Pro678Ala
NM_001207055.1:c.2134C>G	NP_001193984.1:p.Pro712Ala
NM_001207056.1:c.2032C>G	NP_001193985.1:p.Pro678Ala
NM_006892.3:c.2509C>G , LRG_56t1:c.2509C>G	NP_008823.1:p.Pro837Ala
NM_175848.1:c.2449C>G	NP_787044.1:p.Pro817Ala
NM_175849.1:c.2260C>G	NP_787045.1:p.Pro754Ala
NM_175850.2:c.2485C>G	NP_787046.1:p.Pro829Ala
XM_011528653.1:c.2296C>G	XP_011526955.1:p.Pro766Ala
XM_011528654.1:c.2170C>G	XP_011526956.1:p.Pro724Ala
XR_936511.1:n.2287C>G
XM_011528653.2:c.2296C>G	XP_011526955.1:p.Pro766Ala
XM_011528654.2:c.2170C>G	XP_011526956.1:p.Pro724Ala
XR_936511.2:n.2298C>G
NM_001207055.2:c.2134C>G	NP_001193984.1:p.Pro712Ala
NM_001207056.2:c.2032C>G	NP_001193985.1:p.Pro678Ala
NM_006892.4:c.2509C>G MANE Select	NP_008823.1:p.Pro837Ala
NM_175848.2:c.2449C>G	NP_787044.1:p.Pro817Ala
NM_175849.2:c.2260C>G	NP_787045.1:p.Pro754Ala
NM_175850.3:c.2485C>G	NP_787046.1:p.Pro829Ala