Canonical Allele Identifier: CA2499222346
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050378
ClinVar RCV Id: RCV001357733
dbSNP Id: rs2137618829

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379315_32379819del , CM000675.2:g.32379315_32379819del GRCh38
NC_000013.10:g.32953452_32953956del , CM000675.1:g.32953452_32953956del GRCh37
NC_000013.9:g.31851452_31851956del NCBI36
NG_012772.3:g.68836_69340del , LRG_293:g.68836_69340del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8755-2_9023del
ENST00000528762.2:c.*122-2_*390del
ENST00000530893.7:c.8386-2_8654del
ENST00000665585.2:c.*317-2_*585del
ENST00000666593.2:c.8755-2_9023del
ENST00000700202.2:c.8755-2_8972del
ENST00000700202.1:c.1222-2_1439del
ENST00000700203.1:n.882-2_1150del
ENST00000380152.8:c.8755-2_9023del
ENST00000544455.6:c.8755-2_9023del
ENST00000614259.2:c.8763-2_9031del
ENST00000665585.1:c.1633-2_1901del
ENST00000680887.1:c.8755-2_9023del
ENST00000380152.7:c.8755-2_9023del
ENST00000544455.5:c.8755-2_9023del
NM_000059.3:c.8755-2_9023del , LRG_293t1:c.8755-2_9023del
XM_011535203.1:c.8755-2_9023del
XM_011535204.1:c.8659-2_8927del
XM_011535205.1:c.8755-435_*61del
NM_000059.4:c.8755-2_9023del