Canonical Allele Identifier: CA483274514

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 427378
• ClinVar RCV Id: RCV000495224 ; RCV000565515 ; RCV002056816
• dbSNP Id: rs1131692112
• MyVariant Identifiers: chr13:g.32905148A>G (hg19) ; chr13:g.32331011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331011A>G , CM000675.2:g.32331011A>G	GRCh38
NC_000013.10:g.32905148A>G , CM000675.1:g.32905148A>G	GRCh37
NC_000013.9:g.31803148A>G	NCBI36
NG_012772.3:g.20532A>G , LRG_293:g.20532A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.774A>G	ENSP00000434898.2:p.Gln258=
ENST00000528762.2:c.774A>G	ENSP00000433168.2:p.Gln258=
ENST00000530893.7:c.405A>G	ENSP00000499438.2:p.Gln135=
ENST00000665585.2:c.774A>G	ENSP00000499570.2:p.Gln258=
ENST00000666593.2:c.774A>G	ENSP00000499256.2:p.Gln258=
ENST00000700202.2:c.774A>G	ENSP00000514856.2:p.Gln258=
ENST00000700201.1:c.*553A>G	ENSP00000514855.1:n.*553A>G
ENST00000380152.8:c.774A>G MANE Select	ENSP00000369497.3:p.Gln258=
ENST00000544455.6:c.774A>G	ENSP00000439902.1:p.Gln258=
ENST00000614259.2:c.774A>G	ENSP00000506251.1:p.Gln258=
ENST00000680887.1:c.774A>G	ENSP00000505508.1:p.Gln258=
ENST00000380152.7:c.774A>G	ENSP00000369497.3:p.Gln258=
ENST00000530893.6:n.972A>G
ENST00000544455.5:c.774A>G	ENSP00000439902.1:p.Gln258=
ENST00000614259.1:n.774A>G
NM_000059.3:c.774A>G , LRG_293t1:c.774A>G	NP_000050.2:p.Gln258=
XM_011535203.1:c.774A>G	XP_011533505.1:p.Gln258=
XM_011535204.1:c.774A>G	XP_011533506.1:p.Gln258=
XM_011535205.1:c.774A>G	XP_011533507.1:p.Gln258=
NM_000059.4:c.774A>G MANE Select	NP_000050.3:p.Gln258=