Canonical Allele Identifier: CA483271636

Gene: BRCA2

Linked Data

• dbSNP Id: rs2073040676
• MyVariant Identifiers: chr13:g.32971082A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32396945A>T , CM000675.2:g.32396945A>T	GRCh38
NC_000013.10:g.32971082A>T , CM000675.1:g.32971082A>T	GRCh37
NC_000013.9:g.31869082A>T	NCBI36
NG_012772.3:g.86466A>T , LRG_293:g.86466A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*72A>T	ENSP00000434898.2:n.*72A>T
ENST00000528762.2:c.*916A>T	ENSP00000433168.2:n.*916A>T
ENST00000530893.7:c.9180A>T	ENSP00000499438.2:p.Ile3060=
ENST00000665585.2:c.*1111A>T	ENSP00000499570.2:n.*1111A>T
ENST00000700202.2:c.9498A>T	ENSP00000514856.2:p.Ile3166=
ENST00000700202.1:c.1965A>T	ENSP00000514856.1:p.Ile655=
ENST00000700203.1:n.1676A>T
ENST00000380152.8:c.9549A>T MANE Select	ENSP00000369497.3:p.Ile3183=
ENST00000544455.6:c.9549A>T	ENSP00000439902.1:p.Ile3183=
ENST00000614259.2:c.9557A>T	ENSP00000506251.1:n.9557A>T
ENST00000665585.1:c.2427A>T
ENST00000680887.1:c.9549A>T	ENSP00000505508.1:p.Ile3183=
ENST00000380152.7:c.9549A>T	ENSP00000369497.3:p.Ile3183=
ENST00000470094.1:c.632A>T
ENST00000533776.1:n.137A>T
ENST00000544455.5:c.9549A>T	ENSP00000439902.1:p.Ile3183=
NM_000059.3:c.9549A>T , LRG_293t1:c.9549A>T	NP_000050.2:p.Ile3183=
XM_011535203.1:c.9549A>T	XP_011533505.1:p.Ile3183=
XM_011535204.1:c.9453A>T	XP_011533506.1:p.Ile3151=
NM_000059.4:c.9549A>T MANE Select	NP_000050.3:p.Ile3183=