Canonical Allele Identifier: CA483840970

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522193T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948057T>A , CM000675.2:g.50948057T>A	GRCh38
NC_000013.10:g.51522193T>A , CM000675.1:g.51522193T>A	GRCh37
NC_000013.9:g.50420194T>A	NCBI36
NG_009055.1:g.43302T>A , LRG_279:g.43302T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.687T>A MANE Select	ENSP00000337623.2:p.Ser229=
ENST00000422660.6:c.687T>A	ENSP00000389877.1:p.Ser229=
ENST00000459681.3:n.370T>A
ENST00000495244.7:n.698T>A
ENST00000611510.5:c.597T>A	ENSP00000481236.3:p.Ser199=
ENST00000616907.2:c.687T>A	ENSP00000482701.2:p.Ser229=
ENST00000642207.1:c.426T>A
ENST00000642454.1:c.597T>A	ENSP00000494221.1:p.Ser199=
ENST00000642721.1:c.687T>A	ENSP00000495650.1:p.Ser229=
ENST00000642995.1:c.570T>A	ENSP00000493499.1:p.Ser190=
ENST00000643159.1:c.597T>A	ENSP00000495587.1:p.Ser199=
ENST00000643215.1:c.557T>A
ENST00000643405.1:c.335T>A
ENST00000643529.1:c.200T>A
ENST00000643682.1:c.687T>A	ENSP00000493655.1:p.Ser229=
ENST00000643774.1:c.651T>A	ENSP00000495482.1:p.Ser217=
ENST00000644034.1:c.135T>A	ENSP00000495456.1:p.Ser45=
ENST00000644183.1:c.577T>A	ENSP00000495657.1:n.577T>A
ENST00000644297.1:c.*545T>A	ENSP00000495519.1:n.*545T>A
ENST00000644420.1:n.713T>A
ENST00000644425.1:c.638T>A
ENST00000644518.1:c.*554T>A	ENSP00000495793.1:n.*554T>A
ENST00000645188.1:c.678T>A	ENSP00000496224.1:p.Ser226=
ENST00000645201.1:n.84T>A
ENST00000645333.1:n.619T>A
ENST00000645370.1:c.522T>A	ENSP00000494019.1:p.Ser174=
ENST00000645618.1:c.597T>A	ENSP00000495429.1:p.Ser199=
ENST00000645712.1:n.711T>A
ENST00000645912.1:c.25T>A
ENST00000645955.1:c.687T>A	ENSP00000495755.1:p.Ser229=
ENST00000645990.1:c.687T>A	ENSP00000496571.1:p.Ser229=
ENST00000646092.1:c.651T>A	ENSP00000496293.1:p.Ser217=
ENST00000646279.1:n.984T>A
ENST00000646339.1:c.349T>A	ENSP00000495773.1:n.349T>A
ENST00000646709.1:c.597T>A	ENSP00000495278.1:p.Ser199=
ENST00000646731.1:c.678T>A	ENSP00000493828.1:p.Ser226=
ENST00000646960.1:c.687T>A	ENSP00000496481.1:p.Ser229=
ENST00000646964.1:n.1326T>A
ENST00000647387.1:c.597T>A	ENSP00000495487.1:p.Ser199=
ENST00000336617.7:c.687T>A	ENSP00000337623.2:p.Ser229=
ENST00000422660.5:c.687T>A	ENSP00000389877.1:p.Ser229=
ENST00000495244.6:n.698T>A
ENST00000611510.4:c.687T>A	ENSP00000481236.2:p.Ser229=
ENST00000613449.4:n.2749T>A
ENST00000616907.1:c.70T>A
ENST00000621641.1:n.275T>A
NM_001142279.2:c.687T>A , LRG_279t1:c.687T>A	NP_001135751.1:p.Ser229=
NM_024570.3:c.687T>A , LRG_279t2:c.687T>A	NP_078846.2:p.Ser229=
XM_005266524.2:c.687T>A	XP_005266581.1:p.Ser229=
XM_005266525.2:c.687T>A	XP_005266582.1:p.Ser229=
XM_006719867.2:c.669T>A	XP_006719930.1:p.Ser223=
XM_011535229.1:c.687T>A	XP_011533531.1:p.Ser229=
XM_011535230.1:c.687T>A	XP_011533532.1:p.Ser229=
XM_011535231.1:c.687T>A	XP_011533533.1:p.Ser229=
XM_011535232.1:c.525T>A	XP_011533534.1:p.Ser175=
XM_011535233.1:c.279T>A	XP_011533535.1:p.Ser93=
XM_006719867.4:c.669T>A	XP_006719930.1:p.Ser223=
XM_011535230.2:c.687T>A	XP_011533532.1:p.Ser229=
XM_011535231.2:c.687T>A	XP_011533533.1:p.Ser229=
XM_011535233.2:c.279T>A	XP_011533535.1:p.Ser93=
XM_017020747.1:c.687T>A	XP_016876236.1:p.Ser229=
NM_024570.4:c.687T>A MANE Select	NP_078846.2:p.Ser229=