Canonical Allele Identifier: CA387754884

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137613046
• MyVariant Identifiers: chr13:g.32950879C>T (hg19) ; chr13:g.32376742C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376742C>T , CM000675.2:g.32376742C>T	GRCh38
NC_000013.10:g.32950879C>T , CM000675.1:g.32950879C>T	GRCh37
NC_000013.9:g.31848879C>T	NCBI36
NG_012772.3:g.66263C>T , LRG_293:g.66263C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8705C>T	ENSP00000434898.2:p.Ala2902Val
ENST00000528762.2:c.*72C>T	ENSP00000433168.2:n.*72C>T
ENST00000530893.7:c.8336C>T	ENSP00000499438.2:p.Ala2779Val
ENST00000665585.2:c.*267C>T	ENSP00000499570.2:n.*267C>T
ENST00000666593.2:c.8705C>T	ENSP00000499256.2:p.Ala2902Val
ENST00000700202.2:c.8705C>T	ENSP00000514856.2:p.Ala2902Val
ENST00000700202.1:c.1172C>T	ENSP00000514856.1:p.Ala391Val
ENST00000700203.1:n.832C>T
ENST00000380152.8:c.8705C>T MANE Select	ENSP00000369497.3:p.Ala2902Val
ENST00000544455.6:c.8705C>T	ENSP00000439902.1:p.Ala2902Val
ENST00000614259.2:c.8713C>T	ENSP00000506251.1:n.8713C>T
ENST00000665585.1:c.1583C>T
ENST00000680887.1:c.8705C>T	ENSP00000505508.1:p.Ala2902Val
ENST00000380152.7:c.8705C>T	ENSP00000369497.3:p.Ala2902Val
ENST00000528762.1:c.267C>T	ENSP00000433168.1:n.267C>T
ENST00000544455.5:c.8705C>T	ENSP00000439902.1:p.Ala2902Val
NM_000059.3:c.8705C>T , LRG_293t1:c.8705C>T	NP_000050.2:p.Ala2902Val
XM_011535203.1:c.8705C>T	XP_011533505.1:p.Ala2902Val
XM_011535204.1:c.8609C>T	XP_011533506.1:p.Ala2870Val
XM_011535205.1:c.8705C>T	XP_011533507.1:p.Ala2902Val
NM_000059.4:c.8705C>T MANE Select	NP_000050.3:p.Ala2902Val