Canonical Allele Identifier: CA658798088
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531277
dbSNP Id: rs1555289496

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394689del , CM000675.2:g.32394689del GRCh38
NC_000013.10:g.32968826del , CM000675.1:g.32968826del GRCh37
NC_000013.9:g.31866826del NCBI36
NG_012772.3:g.84210del , LRG_293:g.84210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.9257del
ENST00000528762.2:c.*624del
ENST00000530893.7:c.8888del
ENST00000665585.2:c.*819del
ENST00000666593.2:c.*102del
ENST00000700202.2:c.9206del
ENST00000700202.1:c.1673del
ENST00000700203.1:n.1384del
ENST00000380152.8:c.9257del
ENST00000544455.6:c.9257del
ENST00000614259.2:c.9265del
ENST00000665585.1:c.2135del
ENST00000666593.1:c.279del
ENST00000680887.1:c.9257del
ENST00000380152.7:c.9257del
ENST00000470094.1:c.214del
ENST00000544455.5:c.9257del
NM_000059.3:c.9257del , LRG_293t1:c.9257del
XM_011535203.1:c.9257del
XM_011535204.1:c.9161del
NM_000059.4:c.9257del