Canonical Allele Identifier: CA387765833

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137663697
• MyVariant Identifiers: chr13:g.32972422G>C (hg19) ; chr13:g.32398285G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398285G>C , CM000675.2:g.32398285G>C	GRCh38
NC_000013.10:g.32972422G>C , CM000675.1:g.32972422G>C	GRCh37
NC_000013.9:g.31870422G>C	NCBI36
NG_012772.3:g.87806G>C , LRG_293:g.87806G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*295G>C	ENSP00000434898.2:n.*295G>C
ENST00000528762.2:c.*1139G>C	ENSP00000433168.2:n.*1139G>C
ENST00000530893.7:c.9403G>C	ENSP00000499438.2:p.Glu3135Gln
ENST00000665585.2:c.*1334G>C	ENSP00000499570.2:n.*1334G>C
ENST00000700202.2:c.9721G>C	ENSP00000514856.2:p.Glu3241Gln
ENST00000700202.1:c.2188G>C	ENSP00000514856.1:p.Glu730Gln
ENST00000700203.1:n.1899G>C
ENST00000380152.8:c.9772G>C MANE Select	ENSP00000369497.3:p.Glu3258Gln
ENST00000544455.6:c.9772G>C	ENSP00000439902.1:p.Glu3258Gln
ENST00000614259.2:c.9780G>C	ENSP00000506251.1:n.9780G>C
ENST00000680887.1:c.9772G>C	ENSP00000505508.1:p.Glu3258Gln
ENST00000380152.7:c.9772G>C	ENSP00000369497.3:p.Glu3258Gln
ENST00000533776.1:n.360G>C
ENST00000544455.5:c.9772G>C	ENSP00000439902.1:p.Glu3258Gln
NM_000059.3:c.9772G>C , LRG_293t1:c.9772G>C	NP_000050.2:p.Glu3258Gln
XM_011535203.1:c.9772G>C	XP_011533505.1:p.Glu3258Gln
XM_011535204.1:c.9676G>C	XP_011533506.1:p.Glu3226Gln
NM_000059.4:c.9772G>C MANE Select	NP_000050.3:p.Glu3258Gln