Canonical Allele Identifier: CA388258928
Gene: RNASEH2B HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50930686G>T , CM000675.2:g.50930686G>T GRCh38
NC_000013.10:g.51504822G>T , CM000675.1:g.51504822G>T GRCh37
NC_000013.9:g.50402823G>T NCBI36
NG_009055.1:g.25931G>T , LRG_279:g.25931G>T

Transcript Alleles

HGVS Amino-acid change
NM_001142279.2:c.248G>T , LRG_279t1:c.248G>T NP_001135751.1:p.Gly83Val
NM_024570.3:c.248G>T , LRG_279t2:c.248G>T NP_078846.2:p.Gly83Val
XM_005266524.2:c.248G>T XP_005266581.1:p.Gly83Val
XM_005266525.2:c.248G>T XP_005266582.1:p.Gly83Val
XM_006719867.2:c.230G>T XP_006719930.1:p.Gly77Val
XM_011535229.1:c.248G>T XP_011533531.1:p.Gly83Val
XM_011535230.1:c.248G>T XP_011533532.1:p.Gly83Val
XM_011535231.1:c.248G>T XP_011533533.1:p.Gly83Val
XM_011535232.1:c.86G>T XP_011533534.1:p.Gly29Val
XM_011535233.1:c.-366G>T XP_011533535.1:p.=
XM_011535234.1:c.248G>T XP_011533536.1:p.Gly83Val
XM_006719867.4:c.230G>T XP_006719930.1:p.Gly77Val
XM_011535230.2:c.248G>T XP_011533532.1:p.Gly83Val
XM_011535231.2:c.248G>T XP_011533533.1:p.Gly83Val
XM_011535233.2:c.-366G>T XP_011533535.1:p.=
XM_017020747.1:c.248G>T XP_016876236.1:p.Gly83Val
ENST00000336617.7:c.248G>T ENSP00000337623.2:p.Gly83Val
ENST00000422660.5:c.248G>T ENSP00000389877.1:p.Gly83Val
ENST00000459681.2:n.46G>T
ENST00000495244.6:n.259G>T
ENST00000611510.4:c.248G>T ENSP00000481236.2:p.Gly83Val