Canonical Allele Identifier: CA483439974

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 480890
• ClinVar RCV Id: RCV000574939
• dbSNP Id: rs1555290058
• MyVariant Identifiers: chr13:g.32972805T>C (hg19) ; chr13:g.32398668T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398668T>C , CM000675.2:g.32398668T>C	GRCh38
NC_000013.10:g.32972805T>C , CM000675.1:g.32972805T>C	GRCh37
NC_000013.9:g.31870805T>C	NCBI36
NG_012772.3:g.88189T>C , LRG_293:g.88189T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*678T>C	ENSP00000434898.2:n.*678T>C
ENST00000528762.2:c.*1522T>C	ENSP00000433168.2:n.*1522T>C
ENST00000530893.7:c.9786T>C	ENSP00000499438.2:p.Arg3262=
ENST00000665585.2:c.*1717T>C	ENSP00000499570.2:n.*1717T>C
ENST00000700202.2:c.10104T>C	ENSP00000514856.2:p.Arg3368=
ENST00000700202.1:c.2571T>C	ENSP00000514856.1:p.Arg857=
ENST00000700203.1:n.2282T>C
ENST00000380152.8:c.10155T>C MANE Select	ENSP00000369497.3:p.Arg3385=
ENST00000544455.6:c.10155T>C	ENSP00000439902.1:p.Arg3385=
ENST00000614259.2:c.10163T>C	ENSP00000506251.1:n.10163T>C
ENST00000680887.1:c.10155T>C	ENSP00000505508.1:p.Arg3385=
ENST00000380152.7:c.10155T>C	ENSP00000369497.3:p.Arg3385=
ENST00000544455.5:c.10155T>C	ENSP00000439902.1:p.Arg3385=
NM_000059.3:c.10155T>C , LRG_293t1:c.10155T>C	NP_000050.2:p.Arg3385=
XM_011535203.1:c.10155T>C	XP_011533505.1:p.Arg3385=
XM_011535204.1:c.10059T>C	XP_011533506.1:p.Arg3353=
NM_000059.4:c.10155T>C MANE Select	NP_000050.3:p.Arg3385=