Canonical Allele Identifier: CA2082830214
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396941A= , CM000675.2:g.32396941A= GRCh38
NC_000013.10:g.32971078A= , CM000675.1:g.32971078A= GRCh37
NC_000013.9:g.31869078A= NCBI36
NG_012772.3:g.86462A= , LRG_293:g.86462A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*68A= ENSP00000434898.2:n.*68A=
ENST00000528762.2:c.*912A= ENSP00000433168.2:n.*912A=
ENST00000530893.7:c.9176A= ENSP00000499438.2:p.His3059=
ENST00000665585.2:c.*1107A= ENSP00000499570.2:n.*1107A=
ENST00000700202.2:c.9494A= ENSP00000514856.2:p.His3165=
ENST00000700202.1:c.1961A= ENSP00000514856.1:p.His654=
ENST00000700203.1:n.1672A=
ENST00000380152.8:c.9545A= MANE Select ENSP00000369497.3:p.His3182=
ENST00000544455.6:c.9545A= ENSP00000439902.1:p.His3182=
ENST00000614259.2:c.9553A= ENSP00000506251.1:n.9553A=
ENST00000665585.1:c.2423A=
ENST00000680887.1:c.9545A= ENSP00000505508.1:p.His3182=
ENST00000380152.7:c.9545A= ENSP00000369497.3:p.His3182=
ENST00000470094.1:c.628A=
ENST00000533776.1:n.133A=
ENST00000544455.5:c.9545A= ENSP00000439902.1:p.His3182=
NM_000059.3:c.9545A= , LRG_293t1:c.9545A= NP_000050.2:p.His3182=
XM_011535203.1:c.9545A= XP_011533505.1:p.His3182=
XM_011535204.1:c.9449A= XP_011533506.1:p.His3150=
NM_000059.4:c.9545A= MANE Select NP_000050.3:p.His3182=