Canonical Allele Identifier: CA388258917

Gene: RNASEH2B

Identifiers and link-outs to other resources

• MyVariant Identifiers: chr13:g.51504817A>T (hg19) ; chr13:g.50930681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50930681A>T , CM000675.2:g.50930681A>T	GRCh38
NC_000013.10:g.51504817A>T , CM000675.1:g.51504817A>T	GRCh37
NC_000013.9:g.50402818A>T	NCBI36
NG_009055.1:g.25926A>T , LRG_279:g.25926A>T

Transcript Alleles

HGVS	Amino-acid change
NM_001142279.2:c.245-2A>T , LRG_279t1:c.245-2A>T	NP_001135751.1:p.=
NM_024570.3:c.245-2A>T , LRG_279t2:c.245-2A>T	NP_078846.2:p.=
XM_005266524.2:c.245-2A>T	XP_005266581.1:p.=
XM_005266525.2:c.245-2A>T	XP_005266582.1:p.=
XM_006719867.2:c.227-2A>T	XP_006719930.1:p.=
XM_011535229.1:c.245-2A>T	XP_011533531.1:p.=
XM_011535230.1:c.245-2A>T	XP_011533532.1:p.=
XM_011535231.1:c.245-2A>T	XP_011533533.1:p.=
XM_011535232.1:c.83-2A>T	XP_011533534.1:p.=
XM_011535233.1:c.-369-2A>T	XP_011533535.1:p.=
XM_011535234.1:c.245-2A>T	XP_011533536.1:p.=
XM_006719867.4:c.227-2A>T	XP_006719930.1:p.=
XM_011535230.2:c.245-2A>T	XP_011533532.1:p.=
XM_011535231.2:c.245-2A>T	XP_011533533.1:p.=
XM_011535233.2:c.-369-2A>T	XP_011533535.1:p.=
XM_017020747.1:c.245-2A>T	XP_016876236.1:p.=
ENST00000336617.7:c.245-2A>T	ENSP00000337623.2:p.=
ENST00000422660.5:c.245-2A>T	ENSP00000389877.1:p.=
ENST00000459681.2:n.43-2A>T
ENST00000495244.6:n.256-2A>T
ENST00000611510.4:c.245-2A>T	ENSP00000481236.2:p.=