Canonical Allele Identifier: CA609083125

Gene: BRCA2

Linked Data

• dbSNP Id: rs1454505634
• gnomAD v2: 13-32889584-CGCGTCACG-C
• gnomAD v3: 13-32315447-CGCGTCACG-C
• gnomAD v4: 13-32315447-CGCGTCACG-C
• MyVariant Identifiers: chr13:g.32889585_32889592del (hg19) ; chr13:g.32315448_32315455del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315456_32315463del , CM000675.2:g.32315456_32315463del	GRCh38
NC_000013.10:g.32889593_32889600del , CM000675.1:g.32889593_32889600del	GRCh37
NC_000013.9:g.31787593_31787600del	NCBI36
NG_012772.3:g.4977_4984del , LRG_293:g.4977_4984del
NG_017006.1:g.1500_1507del
NG_017006.2:g.4909_4916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544455.6:c.-40+311_-40+318del	ENSP00000439902.1:n.-40+311_-40+318del
XM_011535203.1:c.-40+311_-40+318del	XP_011533505.1:n.-40+311_-40+318del