Canonical Allele Identifier: CA2091111537
Gene: RNASEH2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50947998C= , CM000675.2:g.50947998C= GRCh38
NC_000013.10:g.51522134C= , CM000675.1:g.51522134C= GRCh37
NC_000013.9:g.50420135C= NCBI36
NG_009055.1:g.43243C= , LRG_279:g.43243C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.628C= MANE Select ENSP00000337623.2:p.Arg210=
ENST00000422660.6:c.628C= ENSP00000389877.1:p.Arg210=
ENST00000459681.3:n.311C=
ENST00000495244.7:n.639C=
ENST00000611510.5:c.538C= ENSP00000481236.3:p.Arg180=
ENST00000616907.2:c.628C= ENSP00000482701.2:p.Arg210=
ENST00000642207.1:c.367C=
ENST00000642454.1:c.538C= ENSP00000494221.1:p.Arg180=
ENST00000642721.1:c.628C= ENSP00000495650.1:p.Arg210=
ENST00000642995.1:c.511C= ENSP00000493499.1:p.Arg171=
ENST00000643159.1:c.538C= ENSP00000495587.1:p.Arg180=
ENST00000643215.1:c.498C=
ENST00000643405.1:c.276C=
ENST00000643529.1:c.141C=
ENST00000643682.1:c.628C= ENSP00000493655.1:p.Arg210=
ENST00000643774.1:c.592C= ENSP00000495482.1:p.Arg198=
ENST00000644034.1:c.76C= ENSP00000495456.1:p.Arg26=
ENST00000644183.1:c.518C= ENSP00000495657.1:n.518C=
ENST00000644297.1:c.*486C= ENSP00000495519.1:n.*486C=
ENST00000644420.1:n.654C=
ENST00000644425.1:c.579C=
ENST00000644518.1:c.*495C= ENSP00000495793.1:n.*495C=
ENST00000645188.1:c.619C= ENSP00000496224.1:p.Arg207=
ENST00000645201.1:n.25C=
ENST00000645333.1:n.560C=
ENST00000645370.1:c.463C= ENSP00000494019.1:p.Arg155=
ENST00000645618.1:c.538C= ENSP00000495429.1:p.Arg180=
ENST00000645712.1:n.652C=
ENST00000645955.1:c.628C= ENSP00000495755.1:p.Arg210=
ENST00000645990.1:c.628C= ENSP00000496571.1:p.Arg210=
ENST00000646092.1:c.592C= ENSP00000496293.1:p.Arg198=
ENST00000646279.1:n.925C=
ENST00000646339.1:c.290C= ENSP00000495773.1:n.290C=
ENST00000646709.1:c.538C= ENSP00000495278.1:p.Arg180=
ENST00000646731.1:c.619C= ENSP00000493828.1:p.Arg207=
ENST00000646960.1:c.628C= ENSP00000496481.1:p.Arg210=
ENST00000646964.1:n.1267C=
ENST00000647387.1:c.538C= ENSP00000495487.1:p.Arg180=
ENST00000336617.7:c.628C= ENSP00000337623.2:p.Arg210=
ENST00000422660.5:c.628C= ENSP00000389877.1:p.Arg210=
ENST00000495244.6:n.639C=
ENST00000611510.4:c.628C= ENSP00000481236.2:p.Arg210=
ENST00000613449.4:n.2690C=
ENST00000616907.1:c.11C=
ENST00000621641.1:n.216C=
NM_001142279.2:c.628C= , LRG_279t1:c.628C= NP_001135751.1:p.Arg210=
NM_024570.3:c.628C= , LRG_279t2:c.628C= NP_078846.2:p.Arg210=
XM_005266524.2:c.628C= XP_005266581.1:p.Arg210=
XM_005266525.2:c.628C= XP_005266582.1:p.Arg210=
XM_006719867.2:c.610C= XP_006719930.1:p.Arg204=
XM_011535229.1:c.628C= XP_011533531.1:p.Arg210=
XM_011535230.1:c.628C= XP_011533532.1:p.Arg210=
XM_011535231.1:c.628C= XP_011533533.1:p.Arg210=
XM_011535232.1:c.466C= XP_011533534.1:p.Arg156=
XM_011535233.1:c.220C= XP_011533535.1:p.Arg74=
XM_006719867.4:c.610C= XP_006719930.1:p.Arg204=
XM_011535230.2:c.628C= XP_011533532.1:p.Arg210=
XM_011535231.2:c.628C= XP_011533533.1:p.Arg210=
XM_011535233.2:c.220C= XP_011533535.1:p.Arg74=
XM_017020747.1:c.628C= XP_016876236.1:p.Arg210=
NM_024570.4:c.628C= MANE Select NP_078846.2:p.Arg210=