Canonical Allele Identifier: CA2091111631
Gene: RNASEH2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50948036A= , CM000675.2:g.50948036A= GRCh38
NC_000013.10:g.51522172A= , CM000675.1:g.51522172A= GRCh37
NC_000013.9:g.50420173A= NCBI36
NG_009055.1:g.43281A= , LRG_279:g.43281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.666A= MANE Select ENSP00000337623.2:p.Lys222=
ENST00000422660.6:c.666A= ENSP00000389877.1:p.Lys222=
ENST00000459681.3:n.349A=
ENST00000495244.7:n.677A=
ENST00000611510.5:c.576A= ENSP00000481236.3:p.Lys192=
ENST00000616907.2:c.666A= ENSP00000482701.2:p.Lys222=
ENST00000642207.1:c.405A=
ENST00000642454.1:c.576A= ENSP00000494221.1:p.Lys192=
ENST00000642721.1:c.666A= ENSP00000495650.1:p.Lys222=
ENST00000642995.1:c.549A= ENSP00000493499.1:p.Lys183=
ENST00000643159.1:c.576A= ENSP00000495587.1:p.Lys192=
ENST00000643215.1:c.536A=
ENST00000643405.1:c.314A=
ENST00000643529.1:c.179A=
ENST00000643682.1:c.666A= ENSP00000493655.1:p.Lys222=
ENST00000643774.1:c.630A= ENSP00000495482.1:p.Lys210=
ENST00000644034.1:c.114A= ENSP00000495456.1:p.Lys38=
ENST00000644183.1:c.556A= ENSP00000495657.1:n.556A=
ENST00000644297.1:c.*524A= ENSP00000495519.1:n.*524A=
ENST00000644420.1:n.692A=
ENST00000644425.1:c.617A=
ENST00000644518.1:c.*533A= ENSP00000495793.1:n.*533A=
ENST00000645188.1:c.657A= ENSP00000496224.1:p.Lys219=
ENST00000645201.1:n.63A=
ENST00000645333.1:n.598A=
ENST00000645370.1:c.501A= ENSP00000494019.1:p.Lys167=
ENST00000645618.1:c.576A= ENSP00000495429.1:p.Lys192=
ENST00000645712.1:n.690A=
ENST00000645912.1:c.4A=
ENST00000645955.1:c.666A= ENSP00000495755.1:p.Lys222=
ENST00000645990.1:c.666A= ENSP00000496571.1:p.Lys222=
ENST00000646092.1:c.630A= ENSP00000496293.1:p.Lys210=
ENST00000646279.1:n.963A=
ENST00000646339.1:c.328A= ENSP00000495773.1:n.328A=
ENST00000646709.1:c.576A= ENSP00000495278.1:p.Lys192=
ENST00000646731.1:c.657A= ENSP00000493828.1:p.Lys219=
ENST00000646960.1:c.666A= ENSP00000496481.1:p.Lys222=
ENST00000646964.1:n.1305A=
ENST00000647387.1:c.576A= ENSP00000495487.1:p.Lys192=
ENST00000336617.7:c.666A= ENSP00000337623.2:p.Lys222=
ENST00000422660.5:c.666A= ENSP00000389877.1:p.Lys222=
ENST00000495244.6:n.677A=
ENST00000611510.4:c.666A= ENSP00000481236.2:p.Lys222=
ENST00000613449.4:n.2728A=
ENST00000616907.1:c.49A=
ENST00000621641.1:n.254A=
NM_001142279.2:c.666A= , LRG_279t1:c.666A= NP_001135751.1:p.Lys222=
NM_024570.3:c.666A= , LRG_279t2:c.666A= NP_078846.2:p.Lys222=
XM_005266524.2:c.666A= XP_005266581.1:p.Lys222=
XM_005266525.2:c.666A= XP_005266582.1:p.Lys222=
XM_006719867.2:c.648A= XP_006719930.1:p.Lys216=
XM_011535229.1:c.666A= XP_011533531.1:p.Lys222=
XM_011535230.1:c.666A= XP_011533532.1:p.Lys222=
XM_011535231.1:c.666A= XP_011533533.1:p.Lys222=
XM_011535232.1:c.504A= XP_011533534.1:p.Lys168=
XM_011535233.1:c.258A= XP_011533535.1:p.Lys86=
XM_006719867.4:c.648A= XP_006719930.1:p.Lys216=
XM_011535230.2:c.666A= XP_011533532.1:p.Lys222=
XM_011535231.2:c.666A= XP_011533533.1:p.Lys222=
XM_011535233.2:c.258A= XP_011533535.1:p.Lys86=
XM_017020747.1:c.666A= XP_016876236.1:p.Lys222=
NM_024570.4:c.666A= MANE Select NP_078846.2:p.Lys222=