Canonical Allele Identifier: CA026263
Gene: BRCA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 126217
dbSNP Id: rs80359773

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398185dup , CM000675.2:g.32398185dup GRCh38
NC_000013.10:g.32972322dup , CM000675.1:g.32972322dup GRCh37
NC_000013.9:g.31870322dup NCBI36
NG_012772.3:g.87706dup , LRG_293:g.87706dup

Transcript Alleles

HGVS Amino-acid change
NM_000059.3:c.9672dup , LRG_293t1:c.9672dup NP_000050.2:p.Tyr3225IlefsTer30
XM_011535203.1:c.9672dup XP_011533505.1:p.Tyr3225IlefsTer30
XM_011535204.1:c.9576dup XP_011533506.1:p.Tyr3193IlefsTer30
ENST00000380152.7:c.9672dup ENSP00000369497.3:p.Tyr3225IlefsTer30
ENST00000470094.1:n.755dup
ENST00000533776.1:n.260dup
ENST00000544455.5:c.9672dup ENSP00000439902.1:p.Tyr3225IlefsTer30