Canonical Allele Identifier: CA483261961

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2708664
• ClinVar RCV Id: RCV003530574
• dbSNP Id: rs2137619785
• MyVariant Identifiers: chr13:g.32953546G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379409G>A , CM000675.2:g.32379409G>A	GRCh38
NC_000013.10:g.32953546G>A , CM000675.1:g.32953546G>A	GRCh37
NC_000013.9:g.31851546G>A	NCBI36
NG_012772.3:g.68930G>A , LRG_293:g.68930G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8847G>A	ENSP00000434898.2:p.Arg2949=
ENST00000528762.2:c.*214G>A	ENSP00000433168.2:n.*214G>A
ENST00000530893.7:c.8478G>A	ENSP00000499438.2:p.Arg2826=
ENST00000665585.2:c.*409G>A	ENSP00000499570.2:n.*409G>A
ENST00000666593.2:c.8847G>A	ENSP00000499256.2:p.Arg2949=
ENST00000700202.2:c.8847G>A	ENSP00000514856.2:p.Arg2949=
ENST00000700202.1:c.1314G>A	ENSP00000514856.1:p.Arg438=
ENST00000700203.1:n.974G>A
ENST00000380152.8:c.8847G>A MANE Select	ENSP00000369497.3:p.Arg2949=
ENST00000544455.6:c.8847G>A	ENSP00000439902.1:p.Arg2949=
ENST00000614259.2:c.8855G>A	ENSP00000506251.1:n.8855G>A
ENST00000665585.1:c.1725G>A
ENST00000680887.1:c.8847G>A	ENSP00000505508.1:p.Arg2949=
ENST00000380152.7:c.8847G>A	ENSP00000369497.3:p.Arg2949=
ENST00000528762.1:c.409G>A	ENSP00000433168.1:n.409G>A
ENST00000544455.5:c.8847G>A	ENSP00000439902.1:p.Arg2949=
NM_000059.3:c.8847G>A , LRG_293t1:c.8847G>A	NP_000050.2:p.Arg2949=
XM_011535203.1:c.8847G>A	XP_011533505.1:p.Arg2949=
XM_011535204.1:c.8751G>A	XP_011533506.1:p.Arg2917=
XM_011535205.1:c.8755-341G>A	XP_011533507.1:n.8755-341G>A
NM_000059.4:c.8847G>A MANE Select	NP_000050.3:p.Arg2949=