Canonical Allele Identifier: CA708015656
Gene: RAD51B HGNC NCBI

Linked Data

dbSNP Id: rs1458290715

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564622dup , CM000676.2:g.68564622dup GRCh38
NC_000014.8:g.69031339dup , CM000676.1:g.69031339dup GRCh37
NC_000014.7:g.68101092dup NCBI36
NG_023267.1:g.749831dup
NG_023267.2:g.749844dup

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+96372dup
ENST00000487270.5:c.1037-29863dup ENSP00000419471.1:n.1037-29863dup
ENST00000487861.5:c.1037-46384dup ENSP00000419881.1:n.1037-46384dup
ENST00000488612.5:c.1037-86159dup ENSP00000420061.1:n.1037-86159dup
ENST00000553595.5:n.614-118315dup
ENST00000554244.5:n.487+1004dup
ENST00000556251.1:n.63+18998dup
NM_133509.3:c.1037-29863dup NP_598193.2:n.1037-29863dup
XM_005267963.2:c.1036+96372dup XP_005268020.1:n.1036+96372dup
XM_011537047.1:c.1037-43274dup XP_011535349.1:n.1037-43274dup
XM_011537048.1:c.1037-46384dup XP_011535350.1:n.1037-46384dup
XM_011537049.1:c.*1068dup XP_011535351.1:n.*1068dup
XR_943503.1:n.1407+96372dup
XR_943975.1:n.87+530dup
NM_001321809.1:c.1037-38041dup NP_001308738.1:n.1037-38041dup
NM_001321810.1:c.1037-38041dup NP_001308739.1:n.1037-38041dup
NM_001321815.1:c.923-46536dup NP_001308744.1:n.923-46536dup
NM_001321818.1:c.1036+96372dup NP_001308747.1:n.1036+96372dup
NM_001321821.1:c.1037-46384dup NP_001308750.1:n.1037-46384dup
XM_017021546.1:c.734-46384dup XP_016877035.1:n.734-46384dup
XM_017021547.1:c.680-46384dup XP_016877036.1:n.680-46384dup
XM_017021548.1:c.305-46384dup XP_016877037.1:n.305-46384dup
NM_133509.4:c.1037-29863dup NP_598193.2:n.1037-29863dup
NM_001321809.2:c.1037-38041dup NP_001308738.1:n.1037-38041dup
NM_001321810.2:c.1037-38041dup NP_001308739.1:n.1037-38041dup
NM_001321818.2:c.1036+96372dup NP_001308747.1:n.1036+96372dup
NM_001321821.2:c.1037-46384dup NP_001308750.1:n.1037-46384dup
NM_133509.5:c.1037-29863dup NP_598193.2:n.1037-29863dup