Canonical Allele Identifier: CA388258942
Gene: RNASEH2B HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50930695A>C , CM000675.2:g.50930695A>C GRCh38
NC_000013.10:g.51504831A>C , CM000675.1:g.51504831A>C GRCh37
NC_000013.9:g.50402832A>C NCBI36
NG_009055.1:g.25940A>C , LRG_279:g.25940A>C

Transcript Alleles

HGVS Amino-acid change
NM_001142279.2:c.257A>C , LRG_279t1:c.257A>C NP_001135751.1:p.His86Pro
NM_024570.3:c.257A>C , LRG_279t2:c.257A>C NP_078846.2:p.His86Pro
XM_005266524.2:c.257A>C XP_005266581.1:p.His86Pro
XM_005266525.2:c.257A>C XP_005266582.1:p.His86Pro
XM_006719867.2:c.239A>C XP_006719930.1:p.His80Pro
XM_011535229.1:c.257A>C XP_011533531.1:p.His86Pro
XM_011535230.1:c.257A>C XP_011533532.1:p.His86Pro
XM_011535231.1:c.257A>C XP_011533533.1:p.His86Pro
XM_011535232.1:c.95A>C XP_011533534.1:p.His32Pro
XM_011535233.1:c.-357A>C XP_011533535.1:p.=
XM_011535234.1:c.257A>C XP_011533536.1:p.His86Pro
XM_006719867.4:c.239A>C XP_006719930.1:p.His80Pro
XM_011535230.2:c.257A>C XP_011533532.1:p.His86Pro
XM_011535231.2:c.257A>C XP_011533533.1:p.His86Pro
XM_011535233.2:c.-357A>C XP_011533535.1:p.=
XM_017020747.1:c.257A>C XP_016876236.1:p.His86Pro
ENST00000336617.7:c.257A>C ENSP00000337623.2:p.His86Pro
ENST00000422660.5:c.257A>C ENSP00000389877.1:p.His86Pro
ENST00000459681.2:n.55A>C
ENST00000495244.6:n.268A>C
ENST00000611510.4:c.257A>C ENSP00000481236.2:p.His86Pro