Canonical Allele Identifier: CA387761022

Gene: BRCA2

Linked Data

• dbSNP Id: rs876658469
• MyVariant Identifiers: chr13:g.32968902G>T (hg19) ; chr13:g.32394765G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394765G>T , CM000675.2:g.32394765G>T	GRCh38
NC_000013.10:g.32968902G>T , CM000675.1:g.32968902G>T	GRCh37
NC_000013.9:g.31866902G>T	NCBI36
NG_012772.3:g.84286G>T , LRG_293:g.84286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9333G>T	ENSP00000434898.2:p.Glu3111Asp
ENST00000528762.2:c.*700G>T	ENSP00000433168.2:n.*700G>T
ENST00000530893.7:c.8964G>T	ENSP00000499438.2:p.Glu2988Asp
ENST00000665585.2:c.*895G>T	ENSP00000499570.2:n.*895G>T
ENST00000666593.2:c.*178G>T	ENSP00000499256.2:n.*178G>T
ENST00000700202.2:c.9282G>T	ENSP00000514856.2:p.Glu3094Asp
ENST00000700202.1:c.1749G>T	ENSP00000514856.1:p.Glu583Asp
ENST00000700203.1:n.1460G>T
ENST00000380152.8:c.9333G>T MANE Select	ENSP00000369497.3:p.Glu3111Asp
ENST00000544455.6:c.9333G>T	ENSP00000439902.1:p.Glu3111Asp
ENST00000614259.2:c.9341G>T	ENSP00000506251.1:n.9341G>T
ENST00000665585.1:c.2211G>T
ENST00000666593.1:c.355G>T	ENSP00000499256.1:n.355G>T
ENST00000680887.1:c.9333G>T	ENSP00000505508.1:p.Glu3111Asp
ENST00000380152.7:c.9333G>T	ENSP00000369497.3:p.Glu3111Asp
ENST00000470094.1:c.290G>T
ENST00000544455.5:c.9333G>T	ENSP00000439902.1:p.Glu3111Asp
NM_000059.3:c.9333G>T , LRG_293t1:c.9333G>T	NP_000050.2:p.Glu3111Asp
XM_011535203.1:c.9333G>T	XP_011533505.1:p.Glu3111Asp
XM_011535204.1:c.9237G>T	XP_011533506.1:p.Glu3079Asp
NM_000059.4:c.9333G>T MANE Select	NP_000050.3:p.Glu3111Asp