Canonical Allele Identifier: CA2091101815

Gene: RNASEH2B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50930771G= , CM000675.2:g.50930771G=	GRCh38
NC_000013.10:g.51504907G= , CM000675.1:g.51504907G=	GRCh37
NC_000013.9:g.50402908G=	NCBI36
NG_009055.1:g.26016G= , LRG_279:g.26016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.321+12G= MANE Select	ENSP00000337623.2:n.321+12G=
ENST00000422660.6:c.321+12G=	ENSP00000389877.1:n.321+12G=
ENST00000459681.3:n.119+12G=
ENST00000495244.7:n.332+12G=
ENST00000611510.5:c.231+12G=	ENSP00000481236.3:n.231+12G=
ENST00000616907.2:c.321+12G=	ENSP00000482701.2:n.321+12G=
ENST00000637648.2:c.231+12G=	ENSP00000490077.2:n.231+12G=
ENST00000642207.1:c.175+12G=
ENST00000642454.1:c.231+12G=	ENSP00000494221.1:n.231+12G=
ENST00000642721.1:c.321+12G=	ENSP00000495650.1:n.321+12G=
ENST00000642995.1:c.213+12G=	ENSP00000493499.1:n.213+12G=
ENST00000643159.1:c.231+12G=	ENSP00000495587.1:n.231+12G=
ENST00000643215.1:c.191+12G=
ENST00000643462.1:c.*136+12G=	ENSP00000496130.1:n.*136+12G=
ENST00000643682.1:c.321+12G=	ENSP00000493655.1:n.321+12G=
ENST00000643774.1:c.285+12G=	ENSP00000495482.1:n.285+12G=
ENST00000644034.1:c.65-17216G=	ENSP00000495456.1:n.65-17216G=
ENST00000644183.1:c.211+1189G=	ENSP00000495657.1:n.211+1189G=
ENST00000644297.1:c.*188+12G=	ENSP00000495519.1:n.*188+12G=
ENST00000644420.1:n.347+12G=
ENST00000644425.1:c.272+12G=
ENST00000644518.1:c.*188+12G=	ENSP00000495793.1:n.*188+12G=
ENST00000645188.1:c.321+12G=	ENSP00000496224.1:n.321+12G=
ENST00000645333.1:n.253+12G=
ENST00000645370.1:c.156+12G=	ENSP00000494019.1:n.156+12G=
ENST00000645549.1:n.585+12G=
ENST00000645618.1:c.231+12G=	ENSP00000495429.1:n.231+12G=
ENST00000645712.1:n.354+12G=
ENST00000645955.1:c.321+12G=	ENSP00000495755.1:n.321+12G=
ENST00000645990.1:c.321+12G=	ENSP00000496571.1:n.321+12G=
ENST00000646092.1:c.285+12G=	ENSP00000496293.1:n.285+12G=
ENST00000646279.1:n.618+12G=
ENST00000646339.1:c.21G=	ENSP00000495773.1:p.Gln7=
ENST00000646709.1:c.231+12G=	ENSP00000495278.1:n.231+12G=
ENST00000646731.1:c.321+12G=	ENSP00000493828.1:n.321+12G=
ENST00000646960.1:c.321+12G=	ENSP00000496481.1:n.321+12G=
ENST00000647387.1:c.231+12G=	ENSP00000495487.1:n.231+12G=
ENST00000336617.7:c.321+12G=	ENSP00000337623.2:n.321+12G=
ENST00000422660.5:c.321+12G=	ENSP00000389877.1:n.321+12G=
ENST00000495244.6:n.332+12G=
ENST00000611510.4:c.321+12G=	ENSP00000481236.2:n.321+12G=
NM_001142279.2:c.321+12G= , LRG_279t1:c.321+12G=	NP_001135751.1:n.321+12G=
NM_024570.3:c.321+12G= , LRG_279t2:c.321+12G=	NP_078846.2:n.321+12G=
XM_005266524.2:c.321+12G=	XP_005266581.1:n.321+12G=
XM_005266525.2:c.321+12G=	XP_005266582.1:n.321+12G=
XM_006719867.2:c.303+12G=	XP_006719930.1:n.303+12G=
XM_011535229.1:c.321+12G=	XP_011533531.1:n.321+12G=
XM_011535230.1:c.321+12G=	XP_011533532.1:n.321+12G=
XM_011535231.1:c.321+12G=	XP_011533533.1:n.321+12G=
XM_011535232.1:c.159+12G=	XP_011533534.1:n.159+12G=
XM_011535233.1:c.-293+12G=	XP_011533535.1:n.-293+12G=
XM_011535234.1:c.321+12G=	XP_011533536.1:n.321+12G=
XM_006719867.4:c.303+12G=	XP_006719930.1:n.303+12G=
XM_011535230.2:c.321+12G=	XP_011533532.1:n.321+12G=
XM_011535231.2:c.321+12G=	XP_011533533.1:n.321+12G=
XM_011535233.2:c.-293+12G=	XP_011533535.1:n.-293+12G=
XM_017020747.1:c.321+12G=	XP_016876236.1:n.321+12G=
NM_024570.4:c.321+12G= MANE Select	NP_078846.2:n.321+12G=