Canonical Allele Identifier: CA2082758616
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32330841C= , CM000675.2:g.32330841C= GRCh38
NC_000013.10:g.32904978C= , CM000675.1:g.32904978C= GRCh37
NC_000013.9:g.31802978C= NCBI36
NG_012772.3:g.20362C= , LRG_293:g.20362C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.682-78C= ENSP00000434898.2:n.682-78C=
ENST00000528762.2:c.682-78C= ENSP00000433168.2:n.682-78C=
ENST00000530893.7:c.313-78C= ENSP00000499438.2:n.313-78C=
ENST00000665585.2:c.682-78C= ENSP00000499570.2:n.682-78C=
ENST00000666593.2:c.682-78C= ENSP00000499256.2:n.682-78C=
ENST00000700202.2:c.682-78C= ENSP00000514856.2:n.682-78C=
ENST00000700201.1:c.*461-78C= ENSP00000514855.1:n.*461-78C=
ENST00000380152.8:c.682-78C= MANE Select ENSP00000369497.3:n.682-78C=
ENST00000544455.6:c.682-78C= ENSP00000439902.1:n.682-78C=
ENST00000614259.2:c.682-78C= ENSP00000506251.1:n.682-78C=
ENST00000680887.1:c.682-78C= ENSP00000505508.1:n.682-78C=
ENST00000380152.7:c.682-78C= ENSP00000369497.3:n.682-78C=
ENST00000530893.6:n.880-78C=
ENST00000544455.5:c.682-78C= ENSP00000439902.1:n.682-78C=
ENST00000614259.1:n.682-78C=
NM_000059.3:c.682-78C= , LRG_293t1:c.682-78C= NP_000050.2:n.682-78C=
XM_011535203.1:c.682-78C= XP_011533505.1:n.682-78C=
XM_011535204.1:c.682-78C= XP_011533506.1:n.682-78C=
XM_011535205.1:c.682-78C= XP_011533507.1:n.682-78C=
NM_000059.4:c.682-78C= MANE Select NP_000050.3:n.682-78C=