Canonical Allele Identifier: CA011394
Gene: BRCA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37735
dbSNP Id: rs80359273

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32332743del , CM000675.2:g.32332743del GRCh38
NC_000013.10:g.32906880del , CM000675.1:g.32906880del GRCh37
NC_000013.9:g.31804880del NCBI36
NG_012772.3:g.22264del , LRG_293:g.22264del

Transcript Alleles

HGVS Amino-acid change
NM_000059.3:c.1265del , LRG_293t1:c.1265del NP_000050.2:p.Asn422IlefsTer8
XM_011535203.1:c.1265del XP_011533505.1:p.Asn422IlefsTer8
XM_011535204.1:c.1265del XP_011533506.1:p.Asn422IlefsTer8
XM_011535205.1:c.1265del XP_011533507.1:p.Asn422IlefsTer8
ENST00000380152.7:c.1265del ENSP00000369497.3:p.Asn422IlefsTer8
ENST00000530893.6:n.1463del
ENST00000544455.5:c.1265del ENSP00000439902.1:p.Asn422IlefsTer8
ENST00000614259.1:n.1265del