Canonical Allele Identifier: CA2144362648
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564577G= , CM000676.2:g.68564577G= GRCh38
NC_000014.8:g.69031294G= , CM000676.1:g.69031294G= GRCh37
NC_000014.7:g.68101047G= NCBI36
NG_023267.1:g.749786G=
NG_023267.2:g.749799G=

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+96327G=
ENST00000487270.5:c.1037-29908G= ENSP00000419471.1:n.1037-29908G=
ENST00000487861.5:c.1037-46429G= ENSP00000419881.1:n.1037-46429G=
ENST00000488612.5:c.1037-86204G= ENSP00000420061.1:n.1037-86204G=
ENST00000553595.5:n.614-118360G=
ENST00000554244.5:n.487+959G=
ENST00000556251.1:n.63+18953G=
NM_133509.3:c.1037-29908G= NP_598193.2:n.1037-29908G=
XM_005267963.2:c.1036+96327G= XP_005268020.1:n.1036+96327G=
XM_011537047.1:c.1037-43319G= XP_011535349.1:n.1037-43319G=
XM_011537048.1:c.1037-46429G= XP_011535350.1:n.1037-46429G=
XM_011537049.1:c.*1023G= XP_011535351.1:n.*1023G=
XR_943503.1:n.1407+96327G=
XR_943975.1:n.87+572C=
NM_001321809.1:c.1037-38086G= NP_001308738.1:n.1037-38086G=
NM_001321810.1:c.1037-38086G= NP_001308739.1:n.1037-38086G=
NM_001321815.1:c.923-46581G= NP_001308744.1:n.923-46581G=
NM_001321818.1:c.1036+96327G= NP_001308747.1:n.1036+96327G=
NM_001321821.1:c.1037-46429G= NP_001308750.1:n.1037-46429G=
XM_017021546.1:c.734-46429G= XP_016877035.1:n.734-46429G=
XM_017021547.1:c.680-46429G= XP_016877036.1:n.680-46429G=
XM_017021548.1:c.305-46429G= XP_016877037.1:n.305-46429G=
NM_133509.4:c.1037-29908G= NP_598193.2:n.1037-29908G=
NM_001321809.2:c.1037-38086G= NP_001308738.1:n.1037-38086G=
NM_001321810.2:c.1037-38086G= NP_001308739.1:n.1037-38086G=
NM_001321818.2:c.1036+96327G= NP_001308747.1:n.1036+96327G=
NM_001321821.2:c.1037-46429G= NP_001308750.1:n.1037-46429G=
NM_133509.5:c.1037-29908G= NP_598193.2:n.1037-29908G=