Canonical Allele Identifier: CA2091107511
Gene: RNASEH2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50943376A= , CM000675.2:g.50943376A= GRCh38
NC_000013.10:g.51517512A= , CM000675.1:g.51517512A= GRCh37
NC_000013.9:g.50415513A= NCBI36
NG_009055.1:g.38621A= , LRG_279:g.38621A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.492A= MANE Select ENSP00000337623.2:p.Leu164=
ENST00000422660.6:c.492A= ENSP00000389877.1:p.Leu164=
ENST00000459681.3:n.175A=
ENST00000495244.7:n.503A=
ENST00000611510.5:c.402A= ENSP00000481236.3:p.Leu134=
ENST00000616907.2:c.492A= ENSP00000482701.2:p.Leu164=
ENST00000642207.1:c.231A=
ENST00000642454.1:c.402A= ENSP00000494221.1:p.Leu134=
ENST00000642721.1:c.492A= ENSP00000495650.1:p.Leu164=
ENST00000642995.1:c.375A= ENSP00000493499.1:p.Leu125=
ENST00000643159.1:c.402A= ENSP00000495587.1:p.Leu134=
ENST00000643215.1:c.362A=
ENST00000643405.1:c.140A=
ENST00000643529.1:c.5A=
ENST00000643682.1:c.492A= ENSP00000493655.1:p.Leu164=
ENST00000643774.1:c.456A= ENSP00000495482.1:p.Leu152=
ENST00000644034.1:c.65-4611A= ENSP00000495456.1:n.65-4611A=
ENST00000644183.1:c.382A= ENSP00000495657.1:n.382A=
ENST00000644297.1:c.*350A= ENSP00000495519.1:n.*350A=
ENST00000644420.1:n.518A=
ENST00000644425.1:c.443A=
ENST00000644518.1:c.*359A= ENSP00000495793.1:n.*359A=
ENST00000645188.1:c.483A= ENSP00000496224.1:p.Leu161=
ENST00000645333.1:n.424A=
ENST00000645370.1:c.327A= ENSP00000494019.1:p.Leu109=
ENST00000645618.1:c.402A= ENSP00000495429.1:p.Leu134=
ENST00000645712.1:n.516A=
ENST00000645955.1:c.492A= ENSP00000495755.1:p.Leu164=
ENST00000645990.1:c.492A= ENSP00000496571.1:p.Leu164=
ENST00000646092.1:c.456A= ENSP00000496293.1:p.Leu152=
ENST00000646279.1:n.789A=
ENST00000646339.1:c.154A= ENSP00000495773.1:n.154A=
ENST00000646709.1:c.402A= ENSP00000495278.1:p.Leu134=
ENST00000646731.1:c.483A= ENSP00000493828.1:p.Leu161=
ENST00000646960.1:c.492A= ENSP00000496481.1:p.Leu164=
ENST00000646964.1:n.1131A=
ENST00000647387.1:c.402A= ENSP00000495487.1:p.Leu134=
ENST00000336617.7:c.492A= ENSP00000337623.2:p.Leu164=
ENST00000422660.5:c.492A= ENSP00000389877.1:p.Leu164=
ENST00000495244.6:n.503A=
ENST00000611510.4:c.492A= ENSP00000481236.2:p.Leu164=
ENST00000613449.4:n.2554A=
ENST00000621641.1:n.80A=
NM_001142279.2:c.492A= , LRG_279t1:c.492A= NP_001135751.1:p.Leu164=
NM_024570.3:c.492A= , LRG_279t2:c.492A= NP_078846.2:p.Leu164=
XM_005266524.2:c.492A= XP_005266581.1:p.Leu164=
XM_005266525.2:c.492A= XP_005266582.1:p.Leu164=
XM_006719867.2:c.474A= XP_006719930.1:p.Leu158=
XM_011535229.1:c.492A= XP_011533531.1:p.Leu164=
XM_011535230.1:c.492A= XP_011533532.1:p.Leu164=
XM_011535231.1:c.492A= XP_011533533.1:p.Leu164=
XM_011535232.1:c.330A= XP_011533534.1:p.Leu110=
XM_011535233.1:c.84A= XP_011533535.1:p.Leu28=
XM_011535234.1:c.492A= XP_011533536.1:p.Leu164=
XM_006719867.4:c.474A= XP_006719930.1:p.Leu158=
XM_011535230.2:c.492A= XP_011533532.1:p.Leu164=
XM_011535231.2:c.492A= XP_011533533.1:p.Leu164=
XM_011535233.2:c.84A= XP_011533535.1:p.Leu28=
XM_017020747.1:c.492A= XP_016876236.1:p.Leu164=
NM_024570.4:c.492A= MANE Select NP_078846.2:p.Leu164=