Canonical Allele Identifier: CA2499222047
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1048937
ClinVar RCV Id: RCV001354369
dbSNP Id: rs2137451892

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326497_32326614del , CM000675.2:g.32326497_32326614del GRCh38
NC_000013.10:g.32900634_32900751del , CM000675.1:g.32900634_32900751del GRCh37
NC_000013.9:g.31798634_31798751del NCBI36
NG_012772.3:g.16018_16135del , LRG_293:g.16018_16135del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.517-2_631+1del
ENST00000528762.2:c.517-2_631+1del
ENST00000530893.7:c.148-2_262+1del
ENST00000665585.2:c.517-2_631+1del
ENST00000666593.2:c.517-2_631+1del
ENST00000700202.2:c.517-2_631+1del
ENST00000700200.1:n.388-2_503del
ENST00000700201.1:c.*296-2_*410+1del
ENST00000380152.8:c.517-2_631+1del
ENST00000544455.6:c.517-2_631+1del
ENST00000614259.2:c.517-2_631+1del
ENST00000680887.1:c.517-2_631+1del
ENST00000380152.7:c.517-2_631+1del
ENST00000530893.6:n.715-2_829+1del
ENST00000544455.5:c.517-2_631+1del
ENST00000614259.1:n.517-2_631+1del
NM_000059.3:c.517-2_631+1del , LRG_293t1:c.517-2_631+1del
XM_011535203.1:c.517-2_631+1del
XM_011535204.1:c.517-2_631+1del
XM_011535205.1:c.517-2_631+1del
NM_000059.4:c.517-2_631+1del