Canonical Allele Identifier: CA2082840997
Gene: BRCA2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9227G= ENSP00000434898.2:p.Gly3076=
ENST00000528762.2:c.*594G= ENSP00000433168.2:n.*594G=
ENST00000530893.7:c.8858G= ENSP00000499438.2:p.Gly2953=
ENST00000665585.2:c.*789G= ENSP00000499570.2:n.*789G=
ENST00000666593.2:c.9227G= ENSP00000499256.2:p.Gly3076=
ENST00000700202.2:c.9176G= ENSP00000514856.2:p.Gly3059=
ENST00000700202.1:c.1643G= ENSP00000514856.1:p.Gly548=
ENST00000700203.1:n.1354G=
ENST00000380152.8:c.9227G= MANE Select ENSP00000369497.3:p.Gly3076=
ENST00000544455.6:c.9227G= ENSP00000439902.1:p.Gly3076=
ENST00000614259.2:c.9235G= ENSP00000506251.1:n.9235G=
ENST00000665585.1:c.2105G=
ENST00000666593.1:c.110G= ENSP00000499256.1:p.Gly37=
ENST00000680887.1:c.9227G= ENSP00000505508.1:p.Gly3076=
ENST00000380152.7:c.9227G= ENSP00000369497.3:p.Gly3076=
ENST00000470094.1:c.184G=
ENST00000544455.5:c.9227G= ENSP00000439902.1:p.Gly3076=
NM_000059.3:c.9227G= , LRG_293t1:c.9227G= NP_000050.2:p.Gly3076=
XM_011535203.1:c.9227G= XP_011533505.1:p.Gly3076=
XM_011535204.1:c.9131G= XP_011533506.1:p.Gly3044=
NM_000059.4:c.9227G= MANE Select NP_000050.3:p.Gly3076=