Canonical Allele Identifier: CA15804099
Gene: RAD51B HGNC NCBI

Linked Data

dbSNP Id: rs11624164

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68519440C>T , CM000676.2:g.68519440C>T GRCh38
NC_000014.8:g.68986157C>T , CM000676.1:g.68986157C>T GRCh37
NC_000014.7:g.68055910C>T NCBI36
NG_023267.1:g.704649C>T
NG_023267.2:g.704662C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+51190C>T
ENST00000487270.5:c.1036+51190C>T ENSP00000419471.1:n.1036+51190C>T
ENST00000487861.5:c.1036+51190C>T ENSP00000419881.1:n.1036+51190C>T
ENST00000488612.5:c.1036+51190C>T ENSP00000420061.1:n.1036+51190C>T
ENST00000497460.5:n.497-20760C>T
ENST00000553595.5:n.613+107913C>T
ENST00000554244.5:n.419-44110C>T
NM_133509.3:c.1036+51190C>T NP_598193.2:n.1036+51190C>T
XM_005267963.2:c.1036+51190C>T XP_005268020.1:n.1036+51190C>T
XM_011537047.1:c.1036+51190C>T XP_011535349.1:n.1036+51190C>T
XM_011537048.1:c.1036+51190C>T XP_011535350.1:n.1036+51190C>T
XM_011537049.1:c.1037-44110C>T XP_011535351.1:n.1037-44110C>T
XR_943503.1:n.1407+51190C>T
NM_001321809.1:c.1036+51190C>T NP_001308738.1:n.1036+51190C>T
NM_001321810.1:c.1036+51190C>T NP_001308739.1:n.1036+51190C>T
NM_001321812.1:c.1037-20760C>T NP_001308741.1:n.1037-20760C>T
NM_001321814.1:c.1037-20760C>T NP_001308743.1:n.1037-20760C>T
NM_001321815.1:c.922+51190C>T NP_001308744.1:n.922+51190C>T
NM_001321818.1:c.1036+51190C>T NP_001308747.1:n.1036+51190C>T
NM_001321821.1:c.1036+51190C>T NP_001308750.1:n.1036+51190C>T
XM_017021546.1:c.733+51190C>T XP_016877035.1:n.733+51190C>T
XM_017021547.1:c.679+51190C>T XP_016877036.1:n.679+51190C>T
XM_017021548.1:c.304+51190C>T XP_016877037.1:n.304+51190C>T
NM_133509.4:c.1036+51190C>T NP_598193.2:n.1036+51190C>T
NM_001321809.2:c.1036+51190C>T NP_001308738.1:n.1036+51190C>T
NM_001321810.2:c.1036+51190C>T NP_001308739.1:n.1036+51190C>T
NM_001321814.2:c.1037-20760C>T NP_001308743.1:n.1037-20760C>T
NM_001321818.2:c.1036+51190C>T NP_001308747.1:n.1036+51190C>T
NM_001321821.2:c.1036+51190C>T NP_001308750.1:n.1036+51190C>T
NM_133509.5:c.1036+51190C>T NP_598193.2:n.1036+51190C>T