Canonical Allele Identifier: CA2082834074
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398190A= , CM000675.2:g.32398190A= GRCh38
NC_000013.10:g.32972327A= , CM000675.1:g.32972327A= GRCh37
NC_000013.9:g.31870327A= NCBI36
NG_012772.3:g.87711A= , LRG_293:g.87711A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*200A= ENSP00000434898.2:n.*200A=
ENST00000528762.2:c.*1044A= ENSP00000433168.2:n.*1044A=
ENST00000530893.7:c.9308A= ENSP00000499438.2:p.Tyr3103=
ENST00000665585.2:c.*1239A= ENSP00000499570.2:n.*1239A=
ENST00000700202.2:c.9626A= ENSP00000514856.2:p.Tyr3209=
ENST00000700202.1:c.2093A= ENSP00000514856.1:p.Tyr698=
ENST00000700203.1:n.1804A=
ENST00000380152.8:c.9677A= MANE Select ENSP00000369497.3:p.Tyr3226=
ENST00000544455.6:c.9677A= ENSP00000439902.1:p.Tyr3226=
ENST00000614259.2:c.9685A= ENSP00000506251.1:n.9685A=
ENST00000665585.1:c.2555A=
ENST00000680887.1:c.9677A= ENSP00000505508.1:p.Tyr3226=
ENST00000380152.7:c.9677A= ENSP00000369497.3:p.Tyr3226=
ENST00000470094.1:c.760A=
ENST00000533776.1:n.265A=
ENST00000544455.5:c.9677A= ENSP00000439902.1:p.Tyr3226=
NM_000059.3:c.9677A= , LRG_293t1:c.9677A= NP_000050.2:p.Tyr3226=
XM_011535203.1:c.9677A= XP_011533505.1:p.Tyr3226=
XM_011535204.1:c.9581A= XP_011533506.1:p.Tyr3194=
NM_000059.4:c.9677A= MANE Select NP_000050.3:p.Tyr3226=