Canonical Allele Identifier: CA2082830228
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396942T= , CM000675.2:g.32396942T= GRCh38
NC_000013.10:g.32971079T= , CM000675.1:g.32971079T= GRCh37
NC_000013.9:g.31869079T= NCBI36
NG_012772.3:g.86463T= , LRG_293:g.86463T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*69T= ENSP00000434898.2:n.*69T=
ENST00000528762.2:c.*913T= ENSP00000433168.2:n.*913T=
ENST00000530893.7:c.9177T= ENSP00000499438.2:p.His3059=
ENST00000665585.2:c.*1108T= ENSP00000499570.2:n.*1108T=
ENST00000700202.2:c.9495T= ENSP00000514856.2:p.His3165=
ENST00000700202.1:c.1962T= ENSP00000514856.1:p.His654=
ENST00000700203.1:n.1673T=
ENST00000380152.8:c.9546T= MANE Select ENSP00000369497.3:p.His3182=
ENST00000544455.6:c.9546T= ENSP00000439902.1:p.His3182=
ENST00000614259.2:c.9554T= ENSP00000506251.1:n.9554T=
ENST00000665585.1:c.2424T=
ENST00000680887.1:c.9546T= ENSP00000505508.1:p.His3182=
ENST00000380152.7:c.9546T= ENSP00000369497.3:p.His3182=
ENST00000470094.1:c.629T=
ENST00000533776.1:n.134T=
ENST00000544455.5:c.9546T= ENSP00000439902.1:p.His3182=
NM_000059.3:c.9546T= , LRG_293t1:c.9546T= NP_000050.2:p.His3182=
XM_011535203.1:c.9546T= XP_011533505.1:p.His3182=
XM_011535204.1:c.9450T= XP_011533506.1:p.His3150=
NM_000059.4:c.9546T= MANE Select NP_000050.3:p.His3182=