Canonical Allele Identifier: CA2082836615
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379495C= , CM000675.2:g.32379495C= GRCh38
NC_000013.10:g.32953632C= , CM000675.1:g.32953632C= GRCh37
NC_000013.9:g.31851632C= NCBI36
NG_012772.3:g.69016C= , LRG_293:g.69016C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8933C= ENSP00000434898.2:p.Ser2978=
ENST00000528762.2:c.*300C= ENSP00000433168.2:n.*300C=
ENST00000530893.7:c.8564C= ENSP00000499438.2:p.Ser2855=
ENST00000665585.2:c.*495C= ENSP00000499570.2:n.*495C=
ENST00000666593.2:c.8933C= ENSP00000499256.2:p.Ser2978=
ENST00000700202.2:c.8933C= ENSP00000514856.2:p.Ser2978=
ENST00000700202.1:c.1400C= ENSP00000514856.1:p.Ser467=
ENST00000700203.1:n.1060C=
ENST00000380152.8:c.8933C= MANE Select ENSP00000369497.3:p.Ser2978=
ENST00000544455.6:c.8933C= ENSP00000439902.1:p.Ser2978=
ENST00000614259.2:c.8941C= ENSP00000506251.1:n.8941C=
ENST00000665585.1:c.1811C=
ENST00000680887.1:c.8933C= ENSP00000505508.1:p.Ser2978=
ENST00000380152.7:c.8933C= ENSP00000369497.3:p.Ser2978=
ENST00000528762.1:c.495C= ENSP00000433168.1:n.495C=
ENST00000544455.5:c.8933C= ENSP00000439902.1:p.Ser2978=
NM_000059.3:c.8933C= , LRG_293t1:c.8933C= NP_000050.2:p.Ser2978=
XM_011535203.1:c.8933C= XP_011533505.1:p.Ser2978=
XM_011535204.1:c.8837C= XP_011533506.1:p.Ser2946=
XM_011535205.1:c.8755-255C= XP_011533507.1:n.8755-255C=
NM_000059.4:c.8933C= MANE Select NP_000050.3:p.Ser2978=