Canonical Allele Identifier: CA388259905

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522186A>T (hg19) ; chr13:g.50948050A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948050A>T , CM000675.2:g.50948050A>T	GRCh38
NC_000013.10:g.51522186A>T , CM000675.1:g.51522186A>T	GRCh37
NC_000013.9:g.50420187A>T	NCBI36
NG_009055.1:g.43295A>T , LRG_279:g.43295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.680A>T MANE Select	ENSP00000337623.2:p.Asp227Val
ENST00000422660.6:c.680A>T	ENSP00000389877.1:p.Asp227Val
ENST00000459681.3:n.363A>T
ENST00000495244.7:n.691A>T
ENST00000611510.5:c.590A>T	ENSP00000481236.3:p.Asp197Val
ENST00000616907.2:c.680A>T	ENSP00000482701.2:p.Asp227Val
ENST00000642207.1:c.419A>T
ENST00000642454.1:c.590A>T	ENSP00000494221.1:p.Asp197Val
ENST00000642721.1:c.680A>T	ENSP00000495650.1:p.Asp227Val
ENST00000642995.1:c.563A>T	ENSP00000493499.1:p.Asp188Val
ENST00000643159.1:c.590A>T	ENSP00000495587.1:p.Asp197Val
ENST00000643215.1:c.550A>T
ENST00000643405.1:c.328A>T
ENST00000643529.1:c.193A>T
ENST00000643682.1:c.680A>T	ENSP00000493655.1:p.Asp227Val
ENST00000643774.1:c.644A>T	ENSP00000495482.1:p.Asp215Val
ENST00000644034.1:c.128A>T	ENSP00000495456.1:p.Asp43Val
ENST00000644183.1:c.570A>T	ENSP00000495657.1:n.570A>T
ENST00000644297.1:c.*538A>T	ENSP00000495519.1:n.*538A>T
ENST00000644420.1:n.706A>T
ENST00000644425.1:c.631A>T
ENST00000644518.1:c.*547A>T	ENSP00000495793.1:n.*547A>T
ENST00000645188.1:c.671A>T	ENSP00000496224.1:p.Asp224Val
ENST00000645201.1:n.77A>T
ENST00000645333.1:n.612A>T
ENST00000645370.1:c.515A>T	ENSP00000494019.1:p.Asp172Val
ENST00000645618.1:c.590A>T	ENSP00000495429.1:p.Asp197Val
ENST00000645712.1:n.704A>T
ENST00000645912.1:c.18A>T
ENST00000645955.1:c.680A>T	ENSP00000495755.1:p.Asp227Val
ENST00000645990.1:c.680A>T	ENSP00000496571.1:p.Asp227Val
ENST00000646092.1:c.644A>T	ENSP00000496293.1:p.Asp215Val
ENST00000646279.1:n.977A>T
ENST00000646339.1:c.342A>T	ENSP00000495773.1:n.342A>T
ENST00000646709.1:c.590A>T	ENSP00000495278.1:p.Asp197Val
ENST00000646731.1:c.671A>T	ENSP00000493828.1:p.Asp224Val
ENST00000646960.1:c.680A>T	ENSP00000496481.1:p.Asp227Val
ENST00000646964.1:n.1319A>T
ENST00000647387.1:c.590A>T	ENSP00000495487.1:p.Asp197Val
ENST00000336617.7:c.680A>T	ENSP00000337623.2:p.Asp227Val
ENST00000422660.5:c.680A>T	ENSP00000389877.1:p.Asp227Val
ENST00000495244.6:n.691A>T
ENST00000611510.4:c.680A>T	ENSP00000481236.2:p.Asp227Val
ENST00000613449.4:n.2742A>T
ENST00000616907.1:c.63A>T
ENST00000621641.1:n.268A>T
NM_001142279.2:c.680A>T , LRG_279t1:c.680A>T	NP_001135751.1:p.Asp227Val
NM_024570.3:c.680A>T , LRG_279t2:c.680A>T	NP_078846.2:p.Asp227Val
XM_005266524.2:c.680A>T	XP_005266581.1:p.Asp227Val
XM_005266525.2:c.680A>T	XP_005266582.1:p.Asp227Val
XM_006719867.2:c.662A>T	XP_006719930.1:p.Asp221Val
XM_011535229.1:c.680A>T	XP_011533531.1:p.Asp227Val
XM_011535230.1:c.680A>T	XP_011533532.1:p.Asp227Val
XM_011535231.1:c.680A>T	XP_011533533.1:p.Asp227Val
XM_011535232.1:c.518A>T	XP_011533534.1:p.Asp173Val
XM_011535233.1:c.272A>T	XP_011533535.1:p.Asp91Val
XM_006719867.4:c.662A>T	XP_006719930.1:p.Asp221Val
XM_011535230.2:c.680A>T	XP_011533532.1:p.Asp227Val
XM_011535231.2:c.680A>T	XP_011533533.1:p.Asp227Val
XM_011535233.2:c.272A>T	XP_011533535.1:p.Asp91Val
XM_017020747.1:c.680A>T	XP_016876236.1:p.Asp227Val
NM_024570.4:c.680A>T MANE Select	NP_078846.2:p.Asp227Val