Canonical Allele Identifier: CA025366
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 52454
ClinVar RCV Id: RCV000258458
dbSNP Id: rs397507946
MyVariant Identifiers: chr13:g.32936833_32936834del (hg19) chr13:g.32362696_32362697del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32362696_32362697del , CM000675.2:g.32362696_32362697del GRCh38
NC_000013.10:g.32936833_32936834del , CM000675.1:g.32936833_32936834del GRCh37
NC_000013.9:g.31834833_31834834del NCBI36
NG_012772.3:g.52217_52218del , LRG_293:g.52217_52218del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7976+3_7976+4del ENSP00000434898.2:n.7976+3_7976+4del
ENST00000528762.2:c.7976+3_7976+4del ENSP00000433168.2:n.7976+3_7976+4del
ENST00000530893.7:c.7607+3_7607+4del ENSP00000499438.2:n.7607+3_7607+4del
ENST00000665585.2:c.7976+3_7976+4del ENSP00000499570.2:n.7976+3_7976+4del
ENST00000666593.2:c.7976+3_7976+4del ENSP00000499256.2:n.7976+3_7976+4del
ENST00000700202.2:c.7976+3_7976+4del ENSP00000514856.2:n.7976+3_7976+4del
ENST00000700202.1:c.443+3_443+4del ENSP00000514856.1:n.443+3_443+4del
ENST00000380152.8:c.7976+3_7976+4del MANE Select ENSP00000369497.3:n.7976+3_7976+4del
ENST00000544455.6:c.7976+3_7976+4del ENSP00000439902.1:n.7976+3_7976+4del
ENST00000614259.2:c.7984+3_7984+4del ENSP00000506251.1:n.7984+3_7984+4del
ENST00000665585.1:c.541+3_541+4del
ENST00000680887.1:c.7976+3_7976+4del ENSP00000505508.1:n.7976+3_7976+4del
ENST00000380152.7:c.7976+3_7976+4del ENSP00000369497.3:n.7976+3_7976+4del
ENST00000544455.5:c.7976+3_7976+4del ENSP00000439902.1:n.7976+3_7976+4del
NM_000059.3:c.7976+3_7976+4del , LRG_293t1:c.7976+3_7976+4del NP_000050.2:n.7976+3_7976+4del
XM_011535203.1:c.7976+3_7976+4del XP_011533505.1:n.7976+3_7976+4del
XM_011535204.1:c.7880+3_7880+4del XP_011533506.1:n.7880+3_7880+4del
XM_011535205.1:c.7976+3_7976+4del XP_011533507.1:n.7976+3_7976+4del
NM_000059.4:c.7976+3_7976+4del MANE Select NP_000050.3:n.7976+3_7976+4del
Search 100 bp 5'
Search 100 bp 3'