Canonical Allele Identifier: CA483440010
Gene: BRCA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.32972580A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398443A>T , CM000675.2:g.32398443A>T GRCh38
NC_000013.10:g.32972580A>T , CM000675.1:g.32972580A>T GRCh37
NC_000013.9:g.31870580A>T NCBI36
NG_012772.3:g.87964A>T , LRG_293:g.87964A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*453A>T ENSP00000434898.2:n.*453A>T
ENST00000528762.2:c.*1297A>T ENSP00000433168.2:n.*1297A>T
ENST00000530893.7:c.9561A>T ENSP00000499438.2:p.Thr3187=
ENST00000665585.2:c.*1492A>T ENSP00000499570.2:n.*1492A>T
ENST00000700202.2:c.9879A>T ENSP00000514856.2:p.Thr3293=
ENST00000700202.1:c.2346A>T ENSP00000514856.1:p.Thr782=
ENST00000700203.1:n.2057A>T
ENST00000380152.8:c.9930A>T MANE Select ENSP00000369497.3:p.Thr3310=
ENST00000544455.6:c.9930A>T ENSP00000439902.1:p.Thr3310=
ENST00000614259.2:c.9938A>T ENSP00000506251.1:n.9938A>T
ENST00000680887.1:c.9930A>T ENSP00000505508.1:p.Thr3310=
ENST00000380152.7:c.9930A>T ENSP00000369497.3:p.Thr3310=
ENST00000533776.1:n.518A>T
ENST00000544455.5:c.9930A>T ENSP00000439902.1:p.Thr3310=
NM_000059.3:c.9930A>T , LRG_293t1:c.9930A>T NP_000050.2:p.Thr3310=
XM_011535203.1:c.9930A>T XP_011533505.1:p.Thr3310=
XM_011535204.1:c.9834A>T XP_011533506.1:p.Thr3278=
NM_000059.4:c.9930A>T MANE Select NP_000050.3:p.Thr3310=