Canonical Allele Identifier: CA10586590

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 254624
• ClinVar RCV Id: RCV000241212
• dbSNP Id: rs886038183
• MyVariant Identifiers: chr13:g.32945093_32945094del (hg19) ; chr13:g.32370956_32370957del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370956_32370957del , CM000675.2:g.32370956_32370957del	GRCh38
NC_000013.10:g.32945093_32945094del , CM000675.1:g.32945093_32945094del	GRCh37
NC_000013.9:g.31843093_31843094del	NCBI36
NG_012772.3:g.60477_60478del , LRG_293:g.60477_60478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8488_8489del
ENST00000528762.2:c.8488_8489del
ENST00000530893.7:c.8119_8120del
ENST00000665585.2:c.8488_8489del
ENST00000666593.2:c.8488_8489del
ENST00000700202.2:c.8488_8489del
ENST00000700202.1:c.955_956del
ENST00000380152.8:c.8488_8489del
ENST00000544455.6:c.8488_8489del
ENST00000614259.2:c.8496_8497del
ENST00000665585.1:c.1053_1054del
ENST00000680887.1:c.8488_8489del
ENST00000380152.7:c.8488_8489del
ENST00000544455.5:c.8488_8489del
NM_000059.3:c.8488_8489del , LRG_293t1:c.8488_8489del
XM_011535203.1:c.8488_8489del
XM_011535204.1:c.8392_8393del
XM_011535205.1:c.8488_8489del
NM_000059.4:c.8488_8489del