Canonical Allele Identifier: CA14848371
Gene: DNMT3B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32765121T>C , CM000682.2:g.32765121T>C GRCh38
NC_000020.10:g.31352927T>C , CM000682.1:g.31352927T>C GRCh37
NC_000020.9:g.30816588T>C NCBI36
NG_007290.1:g.7737T>C , LRG_56:g.7737T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.-7+2422T>C ENSP00000512497.1:n.-7+2422T>C
ENST00000696232.1:c.-7+2422T>C ENSP00000512498.1:n.-7+2422T>C
ENST00000696233.1:c.-7+2422T>C ENSP00000512499.1:n.-7+2422T>C
ENST00000696234.1:n.104+2422T>C
ENST00000696235.1:c.-7+2422T>C ENSP00000512500.1:n.-7+2422T>C
ENST00000696236.1:c.-7+2422T>C ENSP00000512501.1:n.-7+2422T>C
ENST00000696237.1:n.100+2260T>C
ENST00000328111.6:c.-7+2422T>C MANE Select ENSP00000328547.2:n.-7+2422T>C
ENST00000348286.6:c.-7+2422T>C ENSP00000337764.2:n.-7+2422T>C
ENST00000353855.6:c.-7+2422T>C ENSP00000313397.4:n.-7+2422T>C
ENST00000443239.7:c.-7+2422T>C ENSP00000403169.2:n.-7+2422T>C
ENST00000456297.6:c.-7+2422T>C ENSP00000412305.1:n.-7+2422T>C
NM_001207055.1:c.-7+2422T>C NP_001193984.1:n.-7+2422T>C
NM_001207056.1:c.-7+2422T>C NP_001193985.1:n.-7+2422T>C
NM_006892.3:c.-7+2422T>C , LRG_56t1:c.-7+2422T>C NP_008823.1:n.-7+2422T>C
NM_175848.1:c.-7+2422T>C NP_787044.1:n.-7+2422T>C
NM_175849.1:c.-7+2422T>C NP_787045.1:n.-7+2422T>C
NM_001207055.2:c.-7+2422T>C NP_001193984.1:n.-7+2422T>C
NM_001207056.2:c.-7+2422T>C NP_001193985.1:n.-7+2422T>C
NM_006892.4:c.-7+2422T>C MANE Select NP_008823.1:n.-7+2422T>C
NM_175848.2:c.-7+2422T>C NP_787044.1:n.-7+2422T>C
NM_175849.2:c.-7+2422T>C NP_787045.1:n.-7+2422T>C
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