Canonical Allele Identifier: CA13941676
Gene: RAD51B HGNC NCBI
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000478014.5:n.384-29169C>T
ENST00000488612.5:c.*11+2912C>T ENSP00000420061.1:n.*11+2912C>T
ENST00000553595.5:n.614-29169C>T
ENST00000554244.5:n.488-29169C>T
XM_005267963.2:c.1037-29169C>T XP_005268020.1:n.1037-29169C>T
XM_011537439.1:c.83-1100G>A XP_011535741.1:n.83-1100G>A
XM_011537440.1:c.83-1100G>A XP_011535742.1:n.83-1100G>A
XR_429374.2:n.1698-1100G>A
XR_943503.1:n.1408-28352C>T
XR_943970.1:n.1698-1100G>A
XR_943972.1:n.1698-1100G>A
XR_943974.1:n.84+1093C>T
NM_001321818.1:c.1037-29169C>T NP_001308747.1:n.1037-29169C>T
NM_001321818.2:c.1037-29169C>T NP_001308747.1:n.1037-29169C>T
Search 100 bp 5'
Search 100 bp 3'