Canonical Allele Identifier: CA483439969

Gene: BRCA2

Linked Data

• dbSNP Id: rs1455620830
• MyVariant Identifiers: chr13:g.32972541A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398404A>T , CM000675.2:g.32398404A>T	GRCh38
NC_000013.10:g.32972541A>T , CM000675.1:g.32972541A>T	GRCh37
NC_000013.9:g.31870541A>T	NCBI36
NG_012772.3:g.87925A>T , LRG_293:g.87925A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*414A>T	ENSP00000434898.2:n.*414A>T
ENST00000528762.2:c.*1258A>T	ENSP00000433168.2:n.*1258A>T
ENST00000530893.7:c.9522A>T	ENSP00000499438.2:p.Ala3174=
ENST00000665585.2:c.*1453A>T	ENSP00000499570.2:n.*1453A>T
ENST00000700202.2:c.9840A>T	ENSP00000514856.2:p.Ala3280=
ENST00000700202.1:c.2307A>T	ENSP00000514856.1:p.Ala769=
ENST00000700203.1:n.2018A>T
ENST00000380152.8:c.9891A>T MANE Select	ENSP00000369497.3:p.Ala3297=
ENST00000544455.6:c.9891A>T	ENSP00000439902.1:p.Ala3297=
ENST00000614259.2:c.9899A>T	ENSP00000506251.1:n.9899A>T
ENST00000680887.1:c.9891A>T	ENSP00000505508.1:p.Ala3297=
ENST00000380152.7:c.9891A>T	ENSP00000369497.3:p.Ala3297=
ENST00000533776.1:n.479A>T
ENST00000544455.5:c.9891A>T	ENSP00000439902.1:p.Ala3297=
NM_000059.3:c.9891A>T , LRG_293t1:c.9891A>T	NP_000050.2:p.Ala3297=
XM_011535203.1:c.9891A>T	XP_011533505.1:p.Ala3297=
XM_011535204.1:c.9795A>T	XP_011533506.1:p.Ala3265=
NM_000059.4:c.9891A>T MANE Select	NP_000050.3:p.Ala3297=