Canonical Allele Identifier: CA387758525

Gene: BRCA2

Linked Data

• dbSNP Id: rs80359187
• MyVariant Identifiers: chr13:g.32954253G>C (hg19) ; chr13:g.32380116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380116G>C , CM000675.2:g.32380116G>C	GRCh38
NC_000013.10:g.32954253G>C , CM000675.1:g.32954253G>C	GRCh37
NC_000013.9:g.31852253G>C	NCBI36
NG_012772.3:g.69637G>C , LRG_293:g.69637G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.9227G>C	ENSP00000434898.2:p.Gly3076Ala
ENST00000528762.2:c.*594G>C	ENSP00000433168.2:n.*594G>C
ENST00000530893.7:c.8858G>C	ENSP00000499438.2:p.Gly2953Ala
ENST00000665585.2:c.*789G>C	ENSP00000499570.2:n.*789G>C
ENST00000666593.2:c.9227G>C	ENSP00000499256.2:p.Gly3076Ala
ENST00000700202.2:c.9176G>C	ENSP00000514856.2:p.Gly3059Ala
ENST00000700202.1:c.1643G>C	ENSP00000514856.1:p.Gly548Ala
ENST00000700203.1:n.1354G>C
ENST00000380152.8:c.9227G>C MANE Select	ENSP00000369497.3:p.Gly3076Ala
ENST00000544455.6:c.9227G>C	ENSP00000439902.1:p.Gly3076Ala
ENST00000614259.2:c.9235G>C	ENSP00000506251.1:n.9235G>C
ENST00000665585.1:c.2105G>C
ENST00000666593.1:c.110G>C	ENSP00000499256.1:p.Gly37Ala
ENST00000680887.1:c.9227G>C	ENSP00000505508.1:p.Gly3076Ala
ENST00000380152.7:c.9227G>C	ENSP00000369497.3:p.Gly3076Ala
ENST00000470094.1:c.184G>C
ENST00000544455.5:c.9227G>C	ENSP00000439902.1:p.Gly3076Ala
NM_000059.3:c.9227G>C , LRG_293t1:c.9227G>C	NP_000050.2:p.Gly3076Ala
XM_011535203.1:c.9227G>C	XP_011533505.1:p.Gly3076Ala
XM_011535204.1:c.9131G>C	XP_011533506.1:p.Gly3044Ala
NM_000059.4:c.9227G>C MANE Select	NP_000050.3:p.Gly3076Ala