Canonical Allele Identifier: CA6940518

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 233895
• ClinVar RCV Id: RCV000220996 ; RCV000499995 ; RCV000657040 ; RCV000757932 ; RCV001798723 ; RCV003998586
• dbSNP Id: rs750341436
• ExAC: 13:32907024 A / C
• gnomAD v2: 13-32907024-A-C
• gnomAD v3: 13-32332887-A-C
• gnomAD v4: 13-32332887-A-C
• MyVariant Identifiers: chr13:g.32907024A>C (hg19) ; chr13:g.32332887A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32332887A>C , CM000675.2:g.32332887A>C	GRCh38
NC_000013.10:g.32907024A>C , CM000675.1:g.32907024A>C	GRCh37
NC_000013.9:g.31805024A>C	NCBI36
NG_012772.3:g.22408A>C , LRG_293:g.22408A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.1409A>C	ENSP00000434898.2:p.Glu470Ala
ENST00000528762.2:c.1409A>C	ENSP00000433168.2:p.Glu470Ala
ENST00000530893.7:c.1040A>C	ENSP00000499438.2:p.Glu347Ala
ENST00000665585.2:c.1409A>C	ENSP00000499570.2:p.Glu470Ala
ENST00000666593.2:c.1409A>C	ENSP00000499256.2:p.Glu470Ala
ENST00000700202.2:c.1409A>C	ENSP00000514856.2:p.Glu470Ala
ENST00000700201.1:c.*1188A>C	ENSP00000514855.1:n.*1188A>C
ENST00000380152.8:c.1409A>C MANE Select	ENSP00000369497.3:p.Glu470Ala
ENST00000544455.6:c.1409A>C	ENSP00000439902.1:p.Glu470Ala
ENST00000614259.2:c.1409A>C	ENSP00000506251.1:p.Glu470Ala
ENST00000680887.1:c.1409A>C	ENSP00000505508.1:p.Glu470Ala
ENST00000380152.7:c.1409A>C	ENSP00000369497.3:p.Glu470Ala
ENST00000530893.6:n.1607A>C
ENST00000544455.5:c.1409A>C	ENSP00000439902.1:p.Glu470Ala
ENST00000614259.1:n.1409A>C
NM_000059.3:c.1409A>C , LRG_293t1:c.1409A>C	NP_000050.2:p.Glu470Ala
XM_011535203.1:c.1409A>C	XP_011533505.1:p.Glu470Ala
XM_011535204.1:c.1409A>C	XP_011533506.1:p.Glu470Ala
XM_011535205.1:c.1409A>C	XP_011533507.1:p.Glu470Ala
NM_000059.4:c.1409A>C MANE Select	NP_000050.3:p.Glu470Ala