Canonical Allele Identifier: CA2580087045
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713207
ClinVar RCV Id: RCV003156002

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32328077_32337667del , CM000675.2:g.32328077_32337667del GRCh38
NC_000013.10:g.32902214_32911804del , CM000675.1:g.32902214_32911804del GRCh37
NC_000013.9:g.31800214_31809804del NCBI36
NG_012772.3:g.17598_27188del , LRG_293:g.17598_27188del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.632-1366_3312del
ENST00000528762.2:c.632-1366_3312del
ENST00000530893.7:c.263-1366_2943del
ENST00000665585.2:c.632-1366_3312del
ENST00000666593.2:c.632-1366_3312del
ENST00000700202.2:c.632-1366_3312del
ENST00000380152.8:c.632-1366_3312del
ENST00000544455.6:c.632-1366_3312del
ENST00000614259.2:c.632-1366_3312del
ENST00000680887.1:c.632-1366_3312del
ENST00000380152.7:c.632-1366_3312del
ENST00000544455.5:c.632-1366_3312del
ENST00000614259.1:n.632-1366_3312del
NM_000059.3:c.632-1366_3312del , LRG_293t1:c.632-1366_3312del
XM_011535203.1:c.632-1366_3312del
XM_011535204.1:c.632-1366_3312del
XM_011535205.1:c.632-1366_3312del
NM_000059.4:c.632-1366_3312del