Canonical Allele Identifier: CA915946976

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 820322
• ClinVar RCV Id: RCV001013657
• dbSNP Id: rs1593895760

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32336264_32336269del , CM000675.2:g.32336264_32336269del	GRCh38
NC_000013.10:g.32910401_32910406del , CM000675.1:g.32910401_32910406del	GRCh37
NC_000013.9:g.31808401_31808406del	NCBI36
NG_012772.3:g.25785_25790del , LRG_293:g.25785_25790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.1910-1_1914del
ENST00000528762.2:c.1910-1_1914del
ENST00000530893.7:c.1541-1_1545del
ENST00000665585.2:c.1910-1_1914del
ENST00000666593.2:c.1910-1_1914del
ENST00000700202.2:c.1910-1_1914del
ENST00000380152.8:c.1910-1_1914del
ENST00000544455.6:c.1910-1_1914del
ENST00000614259.2:c.1910-1_1914del
ENST00000680887.1:c.1910-1_1914del
ENST00000380152.7:c.1910-1_1914del
ENST00000544455.5:c.1910-1_1914del
ENST00000614259.1:n.1910-1_1914del
NM_000059.3:c.1910-1_1914del , LRG_293t1:c.1910-1_1914del
XM_011535203.1:c.1910-1_1914del
XM_011535204.1:c.1910-1_1914del
XM_011535205.1:c.1910-1_1914del
NM_000059.4:c.1910-1_1914del