Canonical Allele Identifier: CA2091111578
Gene: RNASEH2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50948011G= , CM000675.2:g.50948011G= GRCh38
NC_000013.10:g.51522147G= , CM000675.1:g.51522147G= GRCh37
NC_000013.9:g.50420148G= NCBI36
NG_009055.1:g.43256G= , LRG_279:g.43256G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.641G= MANE Select ENSP00000337623.2:p.Gly214=
ENST00000422660.6:c.641G= ENSP00000389877.1:p.Gly214=
ENST00000459681.3:n.324G=
ENST00000495244.7:n.652G=
ENST00000611510.5:c.551G= ENSP00000481236.3:p.Gly184=
ENST00000616907.2:c.641G= ENSP00000482701.2:p.Gly214=
ENST00000642207.1:c.380G=
ENST00000642454.1:c.551G= ENSP00000494221.1:p.Gly184=
ENST00000642721.1:c.641G= ENSP00000495650.1:p.Gly214=
ENST00000642995.1:c.524G= ENSP00000493499.1:p.Gly175=
ENST00000643159.1:c.551G= ENSP00000495587.1:p.Gly184=
ENST00000643215.1:c.511G=
ENST00000643405.1:c.289G=
ENST00000643529.1:c.154G=
ENST00000643682.1:c.641G= ENSP00000493655.1:p.Gly214=
ENST00000643774.1:c.605G= ENSP00000495482.1:p.Gly202=
ENST00000644034.1:c.89G= ENSP00000495456.1:p.Gly30=
ENST00000644183.1:c.531G= ENSP00000495657.1:n.531G=
ENST00000644297.1:c.*499G= ENSP00000495519.1:n.*499G=
ENST00000644420.1:n.667G=
ENST00000644425.1:c.592G=
ENST00000644518.1:c.*508G= ENSP00000495793.1:n.*508G=
ENST00000645188.1:c.632G= ENSP00000496224.1:p.Gly211=
ENST00000645201.1:n.38G=
ENST00000645333.1:n.573G=
ENST00000645370.1:c.476G= ENSP00000494019.1:p.Gly159=
ENST00000645618.1:c.551G= ENSP00000495429.1:p.Gly184=
ENST00000645712.1:n.665G=
ENST00000645955.1:c.641G= ENSP00000495755.1:p.Gly214=
ENST00000645990.1:c.641G= ENSP00000496571.1:p.Gly214=
ENST00000646092.1:c.605G= ENSP00000496293.1:p.Gly202=
ENST00000646279.1:n.938G=
ENST00000646339.1:c.303G= ENSP00000495773.1:n.303G=
ENST00000646709.1:c.551G= ENSP00000495278.1:p.Gly184=
ENST00000646731.1:c.632G= ENSP00000493828.1:p.Gly211=
ENST00000646960.1:c.641G= ENSP00000496481.1:p.Gly214=
ENST00000646964.1:n.1280G=
ENST00000647387.1:c.551G= ENSP00000495487.1:p.Gly184=
ENST00000336617.7:c.641G= ENSP00000337623.2:p.Gly214=
ENST00000422660.5:c.641G= ENSP00000389877.1:p.Gly214=
ENST00000495244.6:n.652G=
ENST00000611510.4:c.641G= ENSP00000481236.2:p.Gly214=
ENST00000613449.4:n.2703G=
ENST00000616907.1:c.24G=
ENST00000621641.1:n.229G=
NM_001142279.2:c.641G= , LRG_279t1:c.641G= NP_001135751.1:p.Gly214=
NM_024570.3:c.641G= , LRG_279t2:c.641G= NP_078846.2:p.Gly214=
XM_005266524.2:c.641G= XP_005266581.1:p.Gly214=
XM_005266525.2:c.641G= XP_005266582.1:p.Gly214=
XM_006719867.2:c.623G= XP_006719930.1:p.Gly208=
XM_011535229.1:c.641G= XP_011533531.1:p.Gly214=
XM_011535230.1:c.641G= XP_011533532.1:p.Gly214=
XM_011535231.1:c.641G= XP_011533533.1:p.Gly214=
XM_011535232.1:c.479G= XP_011533534.1:p.Gly160=
XM_011535233.1:c.233G= XP_011533535.1:p.Gly78=
XM_006719867.4:c.623G= XP_006719930.1:p.Gly208=
XM_011535230.2:c.641G= XP_011533532.1:p.Gly214=
XM_011535231.2:c.641G= XP_011533533.1:p.Gly214=
XM_011535233.2:c.233G= XP_011533535.1:p.Gly78=
XM_017020747.1:c.641G= XP_016876236.1:p.Gly214=
NM_024570.4:c.641G= MANE Select NP_078846.2:p.Gly214=