Canonical Allele Identifier: CA3206689116
Community Standard Title: NC_000014.9:g.68653768C>G
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68653768C>G , CM000676.2:g.68653768C>G GRCh38
NC_000014.8:g.69120485C>G , CM000676.1:g.69120485C>G GRCh37
NC_000014.7:g.68190238C>G NCBI36
NG_023267.2:g.838990C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001321818.1:c.1037-29169C>G NP_001308747.1:n.1037-29169C>G
NM_001321818.2:c.1037-29169C>G NP_001308747.1:n.1037-29169C>G
ENST00000478014.5:n.384-29169C>G
ENST00000488612.5:c.*11+2912C>G ENSP00000420061.1:n.*11+2912C>G
ENST00000553595.5:n.614-29169C>G
ENST00000554244.5:n.488-29169C>G
XM_005267963.2:c.1037-29169C>G XP_005268020.1:n.1037-29169C>G
XM_011537439.1:c.83-1100G>C XP_011535741.1:n.83-1100G>C
XM_011537440.1:c.83-1100G>C XP_011535742.1:n.83-1100G>C
XR_429374.2:n.1698-1100G>C
XR_943503.1:n.1408-28352C>G
XR_943970.1:n.1698-1100G>C
XR_943972.1:n.1698-1100G>C
XR_943974.1:n.84+1093C>G