Canonical Allele Identifier: CA025369
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 52455
dbSNP Id: rs80359027

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32362693G>C , CM000675.2:g.32362693G>C GRCh38
NC_000013.10:g.32936830G>C , CM000675.1:g.32936830G>C GRCh37
NC_000013.9:g.31834830G>C NCBI36
NG_012772.3:g.52214G>C , LRG_293:g.52214G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7976G>C ENSP00000434898.2:p.Arg2659Thr
ENST00000528762.2:c.7976G>C ENSP00000433168.2:p.Arg2659Thr
ENST00000530893.7:c.7607G>C ENSP00000499438.2:p.Arg2536Thr
ENST00000665585.2:c.7976G>C ENSP00000499570.2:p.Arg2659Thr
ENST00000666593.2:c.7976G>C ENSP00000499256.2:p.Arg2659Thr
ENST00000700202.2:c.7976G>C ENSP00000514856.2:p.Arg2659Thr
ENST00000700202.1:c.443G>C ENSP00000514856.1:p.Arg148Thr
ENST00000380152.8:c.7976G>C MANE Select ENSP00000369497.3:p.Arg2659Thr
ENST00000544455.6:c.7976G>C ENSP00000439902.1:p.Arg2659Thr
ENST00000614259.2:c.7984G>C ENSP00000506251.1:n.7984G>C
ENST00000665585.1:c.541G>C
ENST00000680887.1:c.7976G>C ENSP00000505508.1:p.Arg2659Thr
ENST00000380152.7:c.7976G>C ENSP00000369497.3:p.Arg2659Thr
ENST00000544455.5:c.7976G>C ENSP00000439902.1:p.Arg2659Thr
NM_000059.3:c.7976G>C , LRG_293t1:c.7976G>C NP_000050.2:p.Arg2659Thr
XM_011535203.1:c.7976G>C XP_011533505.1:p.Arg2659Thr
XM_011535204.1:c.7880G>C XP_011533506.1:p.Arg2627Thr
XM_011535205.1:c.7976G>C XP_011533507.1:p.Arg2659Thr
NM_000059.4:c.7976G>C MANE Select NP_000050.3:p.Arg2659Thr