Canonical Allele Identifier: CA263391997

Gene: RAD51B

Linked Data

• dbSNP Id: rs763414014
• gnomAD v2: 14-69031346-G-C
• gnomAD v3: 14-68564629-G-C
• gnomAD v4: 14-68564629-G-C
• MyVariant Identifiers: chr14:g.69031346G>C (hg19) ; chr14:g.68564629G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564629G>C , CM000676.2:g.68564629G>C	GRCh38
NC_000014.8:g.69031346G>C , CM000676.1:g.69031346G>C	GRCh37
NC_000014.7:g.68101099G>C	NCBI36
NG_023267.1:g.749838G>C
NG_023267.2:g.749851G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+96379G>C
ENST00000487270.5:c.1037-29856G>C	ENSP00000419471.1:n.1037-29856G>C
ENST00000487861.5:c.1037-46377G>C	ENSP00000419881.1:n.1037-46377G>C
ENST00000488612.5:c.1037-86152G>C	ENSP00000420061.1:n.1037-86152G>C
ENST00000553595.5:n.614-118308G>C
ENST00000554244.5:n.487+1011G>C
ENST00000556251.1:n.63+19005G>C
NM_133509.3:c.1037-29856G>C	NP_598193.2:n.1037-29856G>C
XM_005267963.2:c.1036+96379G>C	XP_005268020.1:n.1036+96379G>C
XM_011537047.1:c.1037-43267G>C	XP_011535349.1:n.1037-43267G>C
XM_011537048.1:c.1037-46377G>C	XP_011535350.1:n.1037-46377G>C
XM_011537049.1:c.*1075G>C	XP_011535351.1:n.*1075G>C
XR_943503.1:n.1407+96379G>C
XR_943975.1:n.87+520C>G
NM_001321809.1:c.1037-38034G>C	NP_001308738.1:n.1037-38034G>C
NM_001321810.1:c.1037-38034G>C	NP_001308739.1:n.1037-38034G>C
NM_001321815.1:c.923-46529G>C	NP_001308744.1:n.923-46529G>C
NM_001321818.1:c.1036+96379G>C	NP_001308747.1:n.1036+96379G>C
NM_001321821.1:c.1037-46377G>C	NP_001308750.1:n.1037-46377G>C
XM_017021546.1:c.734-46377G>C	XP_016877035.1:n.734-46377G>C
XM_017021547.1:c.680-46377G>C	XP_016877036.1:n.680-46377G>C
XM_017021548.1:c.305-46377G>C	XP_016877037.1:n.305-46377G>C
NM_133509.4:c.1037-29856G>C	NP_598193.2:n.1037-29856G>C
NM_001321809.2:c.1037-38034G>C	NP_001308738.1:n.1037-38034G>C
NM_001321810.2:c.1037-38034G>C	NP_001308739.1:n.1037-38034G>C
NM_001321818.2:c.1036+96379G>C	NP_001308747.1:n.1036+96379G>C
NM_001321821.2:c.1037-46377G>C	NP_001308750.1:n.1037-46377G>C
NM_133509.5:c.1037-29856G>C	NP_598193.2:n.1037-29856G>C