Canonical Allele Identifier: CA13941681
Gene: RAD51B HGNC NCBI

Linked Data

dbSNP Id: rs7141529

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68660027T>C , CM000676.2:g.68660027T>C GRCh38
NC_000014.8:g.69126744T>C , CM000676.1:g.69126744T>C GRCh37
NC_000014.7:g.68196497T>C NCBI36
NG_023267.2:g.845249T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478014.5:n.384-22910T>C
ENST00000488612.5:c.*11+9171T>C ENSP00000420061.1:n.*11+9171T>C
ENST00000553595.5:n.614-22910T>C
ENST00000554244.5:n.488-22910T>C
XM_005267963.2:c.1037-22910T>C XP_005268020.1:n.1037-22910T>C
XM_011537439.1:c.83-7359A>G XP_011535741.1:n.83-7359A>G
XM_011537440.1:c.83-7359A>G XP_011535742.1:n.83-7359A>G
XR_429374.2:n.1698-7359A>G
XR_943503.1:n.1408-22093T>C
XR_943970.1:n.1698-7359A>G
XR_943972.1:n.1698-7359A>G
XR_943974.1:n.89+1374T>C
NM_001321818.1:c.1037-22910T>C NP_001308747.1:n.1037-22910T>C
NM_001321818.2:c.1037-22910T>C NP_001308747.1:n.1037-22910T>C