Canonical Allele Identifier: CA263391992

Gene: RAD51B

Linked Data

• dbSNP Id: rs1006616744
• gnomAD v3: 14-68564593-C-T
• gnomAD v4: 14-68564593-C-T
• COSMIC: COSN6257312
• MyVariant Identifiers: chr14:g.69031310C>T (hg19) ; chr14:g.68564593C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564593C>T , CM000676.2:g.68564593C>T	GRCh38
NC_000014.8:g.69031310C>T , CM000676.1:g.69031310C>T	GRCh37
NC_000014.7:g.68101063C>T	NCBI36
NG_023267.1:g.749802C>T
NG_023267.2:g.749815C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+96343C>T
ENST00000487270.5:c.1037-29892C>T	ENSP00000419471.1:n.1037-29892C>T
ENST00000487861.5:c.1037-46413C>T	ENSP00000419881.1:n.1037-46413C>T
ENST00000488612.5:c.1037-86188C>T	ENSP00000420061.1:n.1037-86188C>T
ENST00000553595.5:n.614-118344C>T
ENST00000554244.5:n.487+975C>T
ENST00000556251.1:n.63+18969C>T
NM_133509.3:c.1037-29892C>T	NP_598193.2:n.1037-29892C>T
XM_005267963.2:c.1036+96343C>T	XP_005268020.1:n.1036+96343C>T
XM_011537047.1:c.1037-43303C>T	XP_011535349.1:n.1037-43303C>T
XM_011537048.1:c.1037-46413C>T	XP_011535350.1:n.1037-46413C>T
XM_011537049.1:c.*1039C>T	XP_011535351.1:n.*1039C>T
XR_943503.1:n.1407+96343C>T
XR_943975.1:n.87+556G>A
NM_001321809.1:c.1037-38070C>T	NP_001308738.1:n.1037-38070C>T
NM_001321810.1:c.1037-38070C>T	NP_001308739.1:n.1037-38070C>T
NM_001321815.1:c.923-46565C>T	NP_001308744.1:n.923-46565C>T
NM_001321818.1:c.1036+96343C>T	NP_001308747.1:n.1036+96343C>T
NM_001321821.1:c.1037-46413C>T	NP_001308750.1:n.1037-46413C>T
XM_017021546.1:c.734-46413C>T	XP_016877035.1:n.734-46413C>T
XM_017021547.1:c.680-46413C>T	XP_016877036.1:n.680-46413C>T
XM_017021548.1:c.305-46413C>T	XP_016877037.1:n.305-46413C>T
NM_133509.4:c.1037-29892C>T	NP_598193.2:n.1037-29892C>T
NM_001321809.2:c.1037-38070C>T	NP_001308738.1:n.1037-38070C>T
NM_001321810.2:c.1037-38070C>T	NP_001308739.1:n.1037-38070C>T
NM_001321818.2:c.1036+96343C>T	NP_001308747.1:n.1036+96343C>T
NM_001321821.2:c.1037-46413C>T	NP_001308750.1:n.1037-46413C>T
NM_133509.5:c.1037-29892C>T	NP_598193.2:n.1037-29892C>T