Canonical Allele Identifier: CA313176389
Gene: DNMT3B HGNC NCBI

Linked Data

dbSNP Id: rs6119954
gnomAD v2: 20-31364166-G-A
gnomAD v3: 20-32776360-G-A
gnomAD v4: 20-32776360-G-A
MyVariant Identifiers: chr20:g.31364166G>A (hg19) chr20:g.32776360G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32776360G>A , CM000682.2:g.32776360G>A GRCh38
NC_000020.10:g.31364166G>A , CM000682.1:g.31364166G>A GRCh37
NC_000020.9:g.30827827G>A NCBI36
NG_007290.1:g.18976G>A , LRG_56:g.18976G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696231.1:c.-6-3958G>A ENSP00000512497.1:n.-6-3958G>A
ENST00000696232.1:c.-6-3958G>A ENSP00000512498.1:n.-6-3958G>A
ENST00000696233.1:c.-6-3958G>A ENSP00000512499.1:n.-6-3958G>A
ENST00000696234.1:n.105-3958G>A
ENST00000696235.1:c.-6-3958G>A ENSP00000512500.1:n.-6-3958G>A
ENST00000696236.1:c.-6-3958G>A ENSP00000512501.1:n.-6-3958G>A
ENST00000696237.1:n.101-3958G>A
ENST00000328111.6:c.-6-3958G>A MANE Select ENSP00000328547.2:n.-6-3958G>A
ENST00000348286.6:c.-6-3958G>A ENSP00000337764.2:n.-6-3958G>A
ENST00000353855.6:c.-6-3958G>A ENSP00000313397.4:n.-6-3958G>A
ENST00000443239.7:c.-6-3958G>A ENSP00000403169.2:n.-6-3958G>A
ENST00000456297.6:c.-6-3958G>A ENSP00000412305.1:n.-6-3958G>A
NM_001207055.1:c.-6-3958G>A NP_001193984.1:n.-6-3958G>A
NM_001207056.1:c.-6-3958G>A NP_001193985.1:n.-6-3958G>A
NM_006892.3:c.-6-3958G>A , LRG_56t1:c.-6-3958G>A NP_008823.1:n.-6-3958G>A
NM_175848.1:c.-6-3958G>A NP_787044.1:n.-6-3958G>A
NM_175849.1:c.-6-3958G>A NP_787045.1:n.-6-3958G>A
NM_001207055.2:c.-6-3958G>A NP_001193984.1:n.-6-3958G>A
NM_001207056.2:c.-6-3958G>A NP_001193985.1:n.-6-3958G>A
NM_006892.4:c.-6-3958G>A MANE Select NP_008823.1:n.-6-3958G>A
NM_175848.2:c.-6-3958G>A NP_787044.1:n.-6-3958G>A
NM_175849.2:c.-6-3958G>A NP_787045.1:n.-6-3958G>A
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