Canonical Allele Identifier: CA2144362657
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564601A= , CM000676.2:g.68564601A= GRCh38
NC_000014.8:g.69031318A= , CM000676.1:g.69031318A= GRCh37
NC_000014.7:g.68101071A= NCBI36
NG_023267.1:g.749810A=
NG_023267.2:g.749823A=

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+96351A=
ENST00000487270.5:c.1037-29884A= ENSP00000419471.1:n.1037-29884A=
ENST00000487861.5:c.1037-46405A= ENSP00000419881.1:n.1037-46405A=
ENST00000488612.5:c.1037-86180A= ENSP00000420061.1:n.1037-86180A=
ENST00000553595.5:n.614-118336A=
ENST00000554244.5:n.487+983A=
ENST00000556251.1:n.63+18977A=
NM_133509.3:c.1037-29884A= NP_598193.2:n.1037-29884A=
XM_005267963.2:c.1036+96351A= XP_005268020.1:n.1036+96351A=
XM_011537047.1:c.1037-43295A= XP_011535349.1:n.1037-43295A=
XM_011537048.1:c.1037-46405A= XP_011535350.1:n.1037-46405A=
XM_011537049.1:c.*1047A= XP_011535351.1:n.*1047A=
XR_943503.1:n.1407+96351A=
XR_943975.1:n.87+548T=
NM_001321809.1:c.1037-38062A= NP_001308738.1:n.1037-38062A=
NM_001321810.1:c.1037-38062A= NP_001308739.1:n.1037-38062A=
NM_001321815.1:c.923-46557A= NP_001308744.1:n.923-46557A=
NM_001321818.1:c.1036+96351A= NP_001308747.1:n.1036+96351A=
NM_001321821.1:c.1037-46405A= NP_001308750.1:n.1037-46405A=
XM_017021546.1:c.734-46405A= XP_016877035.1:n.734-46405A=
XM_017021547.1:c.680-46405A= XP_016877036.1:n.680-46405A=
XM_017021548.1:c.305-46405A= XP_016877037.1:n.305-46405A=
NM_133509.4:c.1037-29884A= NP_598193.2:n.1037-29884A=
NM_001321809.2:c.1037-38062A= NP_001308738.1:n.1037-38062A=
NM_001321810.2:c.1037-38062A= NP_001308739.1:n.1037-38062A=
NM_001321818.2:c.1036+96351A= NP_001308747.1:n.1036+96351A=
NM_001321821.2:c.1037-46405A= NP_001308750.1:n.1037-46405A=
NM_133509.5:c.1037-29884A= NP_598193.2:n.1037-29884A=