Canonical Allele Identifier: CA2091107469

Gene: RNASEH2B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50943360G= , CM000675.2:g.50943360G=	GRCh38
NC_000013.10:g.51517496G= , CM000675.1:g.51517496G=	GRCh37
NC_000013.9:g.50415497G=	NCBI36
NG_009055.1:g.38605G= , LRG_279:g.38605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.476G= MANE Select	ENSP00000337623.2:p.Ser159=
ENST00000422660.6:c.476G=	ENSP00000389877.1:p.Ser159=
ENST00000459681.3:n.159G=
ENST00000495244.7:n.487G=
ENST00000611510.5:c.386G=	ENSP00000481236.3:p.Ser129=
ENST00000616907.2:c.476G=	ENSP00000482701.2:p.Ser159=
ENST00000642207.1:c.215G=
ENST00000642454.1:c.386G=	ENSP00000494221.1:p.Ser129=
ENST00000642721.1:c.476G=	ENSP00000495650.1:p.Ser159=
ENST00000642995.1:c.359G=	ENSP00000493499.1:p.Ser120=
ENST00000643159.1:c.386G=	ENSP00000495587.1:p.Ser129=
ENST00000643215.1:c.346G=
ENST00000643405.1:c.124G=
ENST00000643682.1:c.476G=	ENSP00000493655.1:p.Ser159=
ENST00000643774.1:c.440G=	ENSP00000495482.1:p.Ser147=
ENST00000644034.1:c.65-4627G=	ENSP00000495456.1:n.65-4627G=
ENST00000644183.1:c.366G=	ENSP00000495657.1:n.366G=
ENST00000644297.1:c.*334G=	ENSP00000495519.1:n.*334G=
ENST00000644420.1:n.502G=
ENST00000644425.1:c.427G=
ENST00000644518.1:c.*343G=	ENSP00000495793.1:n.*343G=
ENST00000645188.1:c.467G=	ENSP00000496224.1:p.Ser156=
ENST00000645333.1:n.408G=
ENST00000645370.1:c.311G=	ENSP00000494019.1:p.Ser104=
ENST00000645618.1:c.386G=	ENSP00000495429.1:p.Ser129=
ENST00000645712.1:n.500G=
ENST00000645955.1:c.476G=	ENSP00000495755.1:p.Ser159=
ENST00000645990.1:c.476G=	ENSP00000496571.1:p.Ser159=
ENST00000646092.1:c.440G=	ENSP00000496293.1:p.Ser147=
ENST00000646279.1:n.773G=
ENST00000646339.1:c.138G=	ENSP00000495773.1:n.138G=
ENST00000646709.1:c.386G=	ENSP00000495278.1:p.Ser129=
ENST00000646731.1:c.467G=	ENSP00000493828.1:p.Ser156=
ENST00000646960.1:c.476G=	ENSP00000496481.1:p.Ser159=
ENST00000646964.1:n.1115G=
ENST00000647387.1:c.386G=	ENSP00000495487.1:p.Ser129=
ENST00000336617.7:c.476G=	ENSP00000337623.2:p.Ser159=
ENST00000422660.5:c.476G=	ENSP00000389877.1:p.Ser159=
ENST00000495244.6:n.487G=
ENST00000611510.4:c.476G=	ENSP00000481236.2:p.Ser159=
ENST00000613449.4:n.2538G=
ENST00000621641.1:n.64G=
NM_001142279.2:c.476G= , LRG_279t1:c.476G=	NP_001135751.1:p.Ser159=
NM_024570.3:c.476G= , LRG_279t2:c.476G=	NP_078846.2:p.Ser159=
XM_005266524.2:c.476G=	XP_005266581.1:p.Ser159=
XM_005266525.2:c.476G=	XP_005266582.1:p.Ser159=
XM_006719867.2:c.458G=	XP_006719930.1:p.Ser153=
XM_011535229.1:c.476G=	XP_011533531.1:p.Ser159=
XM_011535230.1:c.476G=	XP_011533532.1:p.Ser159=
XM_011535231.1:c.476G=	XP_011533533.1:p.Ser159=
XM_011535232.1:c.314G=	XP_011533534.1:p.Ser105=
XM_011535233.1:c.68G=	XP_011533535.1:p.Ser23=
XM_011535234.1:c.476G=	XP_011533536.1:p.Ser159=
XM_006719867.4:c.458G=	XP_006719930.1:p.Ser153=
XM_011535230.2:c.476G=	XP_011533532.1:p.Ser159=
XM_011535231.2:c.476G=	XP_011533533.1:p.Ser159=
XM_011535233.2:c.68G=	XP_011533535.1:p.Ser23=
XM_017020747.1:c.476G=	XP_016876236.1:p.Ser159=
NM_024570.4:c.476G= MANE Select	NP_078846.2:p.Ser159=