Canonical Allele Identifier: CA2144362605
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564477C= , CM000676.2:g.68564477C= GRCh38
NC_000014.8:g.69031194C= , CM000676.1:g.69031194C= GRCh37
NC_000014.7:g.68100947C= NCBI36
NG_023267.1:g.749686C=
NG_023267.2:g.749699C=

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+96227C=
ENST00000487270.5:c.1037-30008C= ENSP00000419471.1:n.1037-30008C=
ENST00000487861.5:c.1037-46529C= ENSP00000419881.1:n.1037-46529C=
ENST00000488612.5:c.1037-86304C= ENSP00000420061.1:n.1037-86304C=
ENST00000553595.5:n.614-118460C=
ENST00000554244.5:n.487+859C=
ENST00000556251.1:n.63+18853C=
NM_133509.3:c.1037-30008C= NP_598193.2:n.1037-30008C=
XM_005267963.2:c.1036+96227C= XP_005268020.1:n.1036+96227C=
XM_011537047.1:c.1037-43419C= XP_011535349.1:n.1037-43419C=
XM_011537048.1:c.1037-46529C= XP_011535350.1:n.1037-46529C=
XM_011537049.1:c.*923C= XP_011535351.1:n.*923C=
XR_943503.1:n.1407+96227C=
XR_943975.1:n.87+672G=
NM_001321809.1:c.1037-38186C= NP_001308738.1:n.1037-38186C=
NM_001321810.1:c.1037-38186C= NP_001308739.1:n.1037-38186C=
NM_001321815.1:c.923-46681C= NP_001308744.1:n.923-46681C=
NM_001321818.1:c.1036+96227C= NP_001308747.1:n.1036+96227C=
NM_001321821.1:c.1037-46529C= NP_001308750.1:n.1037-46529C=
XM_017021546.1:c.734-46529C= XP_016877035.1:n.734-46529C=
XM_017021547.1:c.680-46529C= XP_016877036.1:n.680-46529C=
XM_017021548.1:c.305-46529C= XP_016877037.1:n.305-46529C=
NM_133509.4:c.1037-30008C= NP_598193.2:n.1037-30008C=
NM_001321809.2:c.1037-38186C= NP_001308738.1:n.1037-38186C=
NM_001321810.2:c.1037-38186C= NP_001308739.1:n.1037-38186C=
NM_001321818.2:c.1036+96227C= NP_001308747.1:n.1036+96227C=
NM_001321821.2:c.1037-46529C= NP_001308750.1:n.1037-46529C=
NM_133509.5:c.1037-30008C= NP_598193.2:n.1037-30008C=