Canonical Allele Identifier: CA387766086

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137663946
• MyVariant Identifiers: chr13:g.32972453G>A (hg19) ; chr13:g.32398316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398316G>A , CM000675.2:g.32398316G>A	GRCh38
NC_000013.10:g.32972453G>A , CM000675.1:g.32972453G>A	GRCh37
NC_000013.9:g.31870453G>A	NCBI36
NG_012772.3:g.87837G>A , LRG_293:g.87837G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*326G>A	ENSP00000434898.2:n.*326G>A
ENST00000528762.2:c.*1170G>A	ENSP00000433168.2:n.*1170G>A
ENST00000530893.7:c.9434G>A	ENSP00000499438.2:p.Arg3145Lys
ENST00000665585.2:c.*1365G>A	ENSP00000499570.2:n.*1365G>A
ENST00000700202.2:c.9752G>A	ENSP00000514856.2:p.Arg3251Lys
ENST00000700202.1:c.2219G>A	ENSP00000514856.1:p.Arg740Lys
ENST00000700203.1:n.1930G>A
ENST00000380152.8:c.9803G>A MANE Select	ENSP00000369497.3:p.Arg3268Lys
ENST00000544455.6:c.9803G>A	ENSP00000439902.1:p.Arg3268Lys
ENST00000614259.2:c.9811G>A	ENSP00000506251.1:n.9811G>A
ENST00000680887.1:c.9803G>A	ENSP00000505508.1:p.Arg3268Lys
ENST00000380152.7:c.9803G>A	ENSP00000369497.3:p.Arg3268Lys
ENST00000533776.1:n.391G>A
ENST00000544455.5:c.9803G>A	ENSP00000439902.1:p.Arg3268Lys
NM_000059.3:c.9803G>A , LRG_293t1:c.9803G>A	NP_000050.2:p.Arg3268Lys
XM_011535203.1:c.9803G>A	XP_011533505.1:p.Arg3268Lys
XM_011535204.1:c.9707G>A	XP_011533506.1:p.Arg3236Lys
NM_000059.4:c.9803G>A MANE Select	NP_000050.3:p.Arg3268Lys