Canonical Allele Identifier: CA1139663038
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 993055
ClinVar RCV Id: RCV001283951

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315482_32316529dup , CM000675.2:g.32315482_32316529dup GRCh38
NC_000013.10:g.32889619_32890666dup , CM000675.1:g.32889619_32890666dup GRCh37
NC_000013.9:g.31787619_31788666dup NCBI36
NG_012772.3:g.5003_6050dup , LRG_293:g.5003_6050dup
NG_017006.1:g.428_1475dup
NG_017006.2:g.3837_4884dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000544455.6:c.-40+337_67+2dup
ENST00000380152.7:c.-225_67+2dup
ENST00000544455.5:c.-225_67+2dup
NM_000059.3:c.-225_67+2dup , LRG_293t1:c.-225_67+2dup
XM_011535203.1:c.-40+337_67+2dup
XM_011535204.1:c.-225_67+2dup
XM_011535205.1:c.-225_67+2dup