Canonical Allele Identifier: CA2082817902
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32339343T= , CM000675.2:g.32339343T= GRCh38
NC_000013.10:g.32913480T= , CM000675.1:g.32913480T= GRCh37
NC_000013.9:g.31811480T= NCBI36
NG_012772.3:g.28864T= , LRG_293:g.28864T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.4988T= ENSP00000434898.2:p.Val1663=
ENST00000528762.2:c.4988T= ENSP00000433168.2:p.Val1663=
ENST00000530893.7:c.4619T= ENSP00000499438.2:p.Val1540=
ENST00000665585.2:c.4988T= ENSP00000499570.2:p.Val1663=
ENST00000666593.2:c.4988T= ENSP00000499256.2:p.Val1663=
ENST00000700202.2:c.4988T= ENSP00000514856.2:p.Val1663=
ENST00000380152.8:c.4988T= MANE Select ENSP00000369497.3:p.Val1663=
ENST00000544455.6:c.4988T= ENSP00000439902.1:p.Val1663=
ENST00000614259.2:c.4988T= ENSP00000506251.1:p.Val1663=
ENST00000680887.1:c.4988T= ENSP00000505508.1:p.Val1663=
ENST00000380152.7:c.4988T= ENSP00000369497.3:p.Val1663=
ENST00000544455.5:c.4988T= ENSP00000439902.1:p.Val1663=
ENST00000614259.1:n.4988T=
NM_000059.3:c.4988T= , LRG_293t1:c.4988T= NP_000050.2:p.Val1663=
XM_011535203.1:c.4988T= XP_011533505.1:p.Val1663=
XM_011535204.1:c.4988T= XP_011533506.1:p.Val1663=
XM_011535205.1:c.4988T= XP_011533507.1:p.Val1663=
NM_000059.4:c.4988T= MANE Select NP_000050.3:p.Val1663=