Canonical Allele Identifier: CA388259861

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522167C>A (hg19) ; chr13:g.50948031C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948031C>A , CM000675.2:g.50948031C>A	GRCh38
NC_000013.10:g.51522167C>A , CM000675.1:g.51522167C>A	GRCh37
NC_000013.9:g.50420168C>A	NCBI36
NG_009055.1:g.43276C>A , LRG_279:g.43276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.661C>A MANE Select	ENSP00000337623.2:p.Pro221Thr
ENST00000422660.6:c.661C>A	ENSP00000389877.1:p.Pro221Thr
ENST00000459681.3:n.344C>A
ENST00000495244.7:n.672C>A
ENST00000611510.5:c.571C>A	ENSP00000481236.3:p.Pro191Thr
ENST00000616907.2:c.661C>A	ENSP00000482701.2:p.Pro221Thr
ENST00000642207.1:c.400C>A
ENST00000642454.1:c.571C>A	ENSP00000494221.1:p.Pro191Thr
ENST00000642721.1:c.661C>A	ENSP00000495650.1:p.Pro221Thr
ENST00000642995.1:c.544C>A	ENSP00000493499.1:p.Pro182Thr
ENST00000643159.1:c.571C>A	ENSP00000495587.1:p.Pro191Thr
ENST00000643215.1:c.531C>A
ENST00000643405.1:c.309C>A
ENST00000643529.1:c.174C>A
ENST00000643682.1:c.661C>A	ENSP00000493655.1:p.Pro221Thr
ENST00000643774.1:c.625C>A	ENSP00000495482.1:p.Pro209Thr
ENST00000644034.1:c.109C>A	ENSP00000495456.1:p.Pro37Thr
ENST00000644183.1:c.551C>A	ENSP00000495657.1:n.551C>A
ENST00000644297.1:c.*519C>A	ENSP00000495519.1:n.*519C>A
ENST00000644420.1:n.687C>A
ENST00000644425.1:c.612C>A
ENST00000644518.1:c.*528C>A	ENSP00000495793.1:n.*528C>A
ENST00000645188.1:c.652C>A	ENSP00000496224.1:p.Pro218Thr
ENST00000645201.1:n.58C>A
ENST00000645333.1:n.593C>A
ENST00000645370.1:c.496C>A	ENSP00000494019.1:p.Pro166Thr
ENST00000645618.1:c.571C>A	ENSP00000495429.1:p.Pro191Thr
ENST00000645712.1:n.685C>A
ENST00000645955.1:c.661C>A	ENSP00000495755.1:p.Pro221Thr
ENST00000645990.1:c.661C>A	ENSP00000496571.1:p.Pro221Thr
ENST00000646092.1:c.625C>A	ENSP00000496293.1:p.Pro209Thr
ENST00000646279.1:n.958C>A
ENST00000646339.1:c.323C>A	ENSP00000495773.1:n.323C>A
ENST00000646709.1:c.571C>A	ENSP00000495278.1:p.Pro191Thr
ENST00000646731.1:c.652C>A	ENSP00000493828.1:p.Pro218Thr
ENST00000646960.1:c.661C>A	ENSP00000496481.1:p.Pro221Thr
ENST00000646964.1:n.1300C>A
ENST00000647387.1:c.571C>A	ENSP00000495487.1:p.Pro191Thr
ENST00000336617.7:c.661C>A	ENSP00000337623.2:p.Pro221Thr
ENST00000422660.5:c.661C>A	ENSP00000389877.1:p.Pro221Thr
ENST00000495244.6:n.672C>A
ENST00000611510.4:c.661C>A	ENSP00000481236.2:p.Pro221Thr
ENST00000613449.4:n.2723C>A
ENST00000616907.1:c.44C>A
ENST00000621641.1:n.249C>A
NM_001142279.2:c.661C>A , LRG_279t1:c.661C>A	NP_001135751.1:p.Pro221Thr
NM_024570.3:c.661C>A , LRG_279t2:c.661C>A	NP_078846.2:p.Pro221Thr
XM_005266524.2:c.661C>A	XP_005266581.1:p.Pro221Thr
XM_005266525.2:c.661C>A	XP_005266582.1:p.Pro221Thr
XM_006719867.2:c.643C>A	XP_006719930.1:p.Pro215Thr
XM_011535229.1:c.661C>A	XP_011533531.1:p.Pro221Thr
XM_011535230.1:c.661C>A	XP_011533532.1:p.Pro221Thr
XM_011535231.1:c.661C>A	XP_011533533.1:p.Pro221Thr
XM_011535232.1:c.499C>A	XP_011533534.1:p.Pro167Thr
XM_011535233.1:c.253C>A	XP_011533535.1:p.Pro85Thr
XM_006719867.4:c.643C>A	XP_006719930.1:p.Pro215Thr
XM_011535230.2:c.661C>A	XP_011533532.1:p.Pro221Thr
XM_011535231.2:c.661C>A	XP_011533533.1:p.Pro221Thr
XM_011535233.2:c.253C>A	XP_011533535.1:p.Pro85Thr
XM_017020747.1:c.661C>A	XP_016876236.1:p.Pro221Thr
NM_024570.4:c.661C>A MANE Select	NP_078846.2:p.Pro221Thr