Canonical Allele Identifier: CA388259874

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522173G>C (hg19) ; chr13:g.50948037G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948037G>C , CM000675.2:g.50948037G>C	GRCh38
NC_000013.10:g.51522173G>C , CM000675.1:g.51522173G>C	GRCh37
NC_000013.9:g.50420174G>C	NCBI36
NG_009055.1:g.43282G>C , LRG_279:g.43282G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.667G>C MANE Select	ENSP00000337623.2:p.Glu223Gln
ENST00000422660.6:c.667G>C	ENSP00000389877.1:p.Glu223Gln
ENST00000459681.3:n.350G>C
ENST00000495244.7:n.678G>C
ENST00000611510.5:c.577G>C	ENSP00000481236.3:p.Glu193Gln
ENST00000616907.2:c.667G>C	ENSP00000482701.2:p.Glu223Gln
ENST00000642207.1:c.406G>C
ENST00000642454.1:c.577G>C	ENSP00000494221.1:p.Glu193Gln
ENST00000642721.1:c.667G>C	ENSP00000495650.1:p.Glu223Gln
ENST00000642995.1:c.550G>C	ENSP00000493499.1:p.Glu184Gln
ENST00000643159.1:c.577G>C	ENSP00000495587.1:p.Glu193Gln
ENST00000643215.1:c.537G>C
ENST00000643405.1:c.315G>C
ENST00000643529.1:c.180G>C
ENST00000643682.1:c.667G>C	ENSP00000493655.1:p.Glu223Gln
ENST00000643774.1:c.631G>C	ENSP00000495482.1:p.Glu211Gln
ENST00000644034.1:c.115G>C	ENSP00000495456.1:p.Glu39Gln
ENST00000644183.1:c.557G>C	ENSP00000495657.1:n.557G>C
ENST00000644297.1:c.*525G>C	ENSP00000495519.1:n.*525G>C
ENST00000644420.1:n.693G>C
ENST00000644425.1:c.618G>C
ENST00000644518.1:c.*534G>C	ENSP00000495793.1:n.*534G>C
ENST00000645188.1:c.658G>C	ENSP00000496224.1:p.Glu220Gln
ENST00000645201.1:n.64G>C
ENST00000645333.1:n.599G>C
ENST00000645370.1:c.502G>C	ENSP00000494019.1:p.Glu168Gln
ENST00000645618.1:c.577G>C	ENSP00000495429.1:p.Glu193Gln
ENST00000645712.1:n.691G>C
ENST00000645912.1:c.5G>C
ENST00000645955.1:c.667G>C	ENSP00000495755.1:p.Glu223Gln
ENST00000645990.1:c.667G>C	ENSP00000496571.1:p.Glu223Gln
ENST00000646092.1:c.631G>C	ENSP00000496293.1:p.Glu211Gln
ENST00000646279.1:n.964G>C
ENST00000646339.1:c.329G>C	ENSP00000495773.1:n.329G>C
ENST00000646709.1:c.577G>C	ENSP00000495278.1:p.Glu193Gln
ENST00000646731.1:c.658G>C	ENSP00000493828.1:p.Glu220Gln
ENST00000646960.1:c.667G>C	ENSP00000496481.1:p.Glu223Gln
ENST00000646964.1:n.1306G>C
ENST00000647387.1:c.577G>C	ENSP00000495487.1:p.Glu193Gln
ENST00000336617.7:c.667G>C	ENSP00000337623.2:p.Glu223Gln
ENST00000422660.5:c.667G>C	ENSP00000389877.1:p.Glu223Gln
ENST00000495244.6:n.678G>C
ENST00000611510.4:c.667G>C	ENSP00000481236.2:p.Glu223Gln
ENST00000613449.4:n.2729G>C
ENST00000616907.1:c.50G>C
ENST00000621641.1:n.255G>C
NM_001142279.2:c.667G>C , LRG_279t1:c.667G>C	NP_001135751.1:p.Glu223Gln
NM_024570.3:c.667G>C , LRG_279t2:c.667G>C	NP_078846.2:p.Glu223Gln
XM_005266524.2:c.667G>C	XP_005266581.1:p.Glu223Gln
XM_005266525.2:c.667G>C	XP_005266582.1:p.Glu223Gln
XM_006719867.2:c.649G>C	XP_006719930.1:p.Glu217Gln
XM_011535229.1:c.667G>C	XP_011533531.1:p.Glu223Gln
XM_011535230.1:c.667G>C	XP_011533532.1:p.Glu223Gln
XM_011535231.1:c.667G>C	XP_011533533.1:p.Glu223Gln
XM_011535232.1:c.505G>C	XP_011533534.1:p.Glu169Gln
XM_011535233.1:c.259G>C	XP_011533535.1:p.Glu87Gln
XM_006719867.4:c.649G>C	XP_006719930.1:p.Glu217Gln
XM_011535230.2:c.667G>C	XP_011533532.1:p.Glu223Gln
XM_011535231.2:c.667G>C	XP_011533533.1:p.Glu223Gln
XM_011535233.2:c.259G>C	XP_011533535.1:p.Glu87Gln
XM_017020747.1:c.667G>C	XP_016876236.1:p.Glu223Gln
NM_024570.4:c.667G>C MANE Select	NP_078846.2:p.Glu223Gln